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C1=CC=C(C=C1)CNCC(C(F)(F)F)O产品信息
3-(苄氨基)-1,1,1-三氟丙-2-醇（CAS 178218-36-5）的产品身份、结构标识及相关反应资料，供化学中间体检索、研发和采购评估使用。
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12 条反应 · 12 篇文献
反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Starting material: benzylamine and 2-(trifluoromethyl)oxirane
来源 ID: ord-72a0ed4de4964b35bec4b347589b987a反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Starting material: benzylamine and 2-(trifluoromethyl)oxirane
来源 ID: ord-72a0ed4de4964b35bec4b347589b987a反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Starting material: benzylamine and 2-(trifluoromethyl)oxirane
来源 ID: ord-1462ed97ac0c4e36bccc605e1b15eb07反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Starting material: benzylamine and 2-(trifluoromethyl)oxirane
来源 ID: ord-1462ed97ac0c4e36bccc605e1b15eb07反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Starting material: benzylamine and 2-(trifluoromethyl)oxirane
来源 ID: ord-72a0ed4de4964b35bec4b347589b987a反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of 3-(Benzylamino)-1,1,1-trifluoropropan-2-ol (2.68 g, 12.3 mmol) and triethylamine (1.7 mL, 12.2 mmol) in CH2Cl2 is cooled to 0° C. The solution is treated drop wise with 2-bromopropanoyl chloride (1.2 mL, 12 mmol, Aldrich) and stirred for 5 minutes. The solution is diluted to 100 mL with CH2Cl2 and washed sequentially with 1.0M HCl, saturated NaHCO3, and brine (100 mL each). The organic layer is dried over Na2SO4 and filtered. The solvent is removed by rotary evaporation yielding (N-benzyl-2-bromo-N-(3,3,3-trifluoro-2-hydroxypropyl)propanamide as a golden oil. Dry NaH is suspended in dry, inhibitor free THF (25 ml) in a flame dried flask and the mixture is cooled to 0° C. with stirring on an ice bath. The N-benzyl-2-bromo-N-(3,3,3-trifluoro-2-hydroxypropyl)propanamide (4.25 g, 12 mmol) is added as a solution in dry, inhibitor free THF (25 ml) and the resultant suspension is warmed to RT. After stirring for one hour the reaction is quenched with MeOH over an ice bath until no more gas evolved and the mixture is poured into 1.0M HCl (200 mL). The aqueous mixture is extracted into MTBE (200 mL) and the organic layer is washed with saturated NaHCO3 and brine (200 mL each). The organic layer is dried over Na2SO4 and filtered, and the solvent is removed by rotary evaporation yielding an amber oil. washed sequentially with 1.0M HCl, saturated NaHCO3, and brine (100 mL each) The organic layer is dried over Na2SO4 filtered The solvent is removed by rotary evaporation
来源 ID: ord-f3a729f80b6c405f9cb23b7d329774d5反应条件: temp:-10.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Lithium triflate was suspended in CH3CN (15 mL) and the mixture is cooled to −10° C. 2-(Trifluoromethyl)oxirane is added and the suspension is allowed to warm to RT with stirring. Benzylamine (6.33 mL, 58 mmol, Aldrich) is added all-at-once and the resultant solution is stirred for 25 minutes. The reaction is quenched by pouring into CH2Cl2 (200 mL) and washing 3× with H2O (200 mL). The organic layer is dried over Na2SO4 and filtered. The product is purified on a Biotage Flash 75L using 20:70:10 CH2Cl2: pentane: triethylamine as eluent. The product containing fractions are pooled and the solvent is removed by rotary evaporation. The product is dried under vacuum at 100° C. yielding a white crystalline solid. to warm to RT is stirred for 25 minutes The reaction is quenched by pouring into CH2Cl2 (200 mL) washing 3× with H2O (200 mL) The organic layer is dried over Na2SO4 filtered The product is purified on a Biotage Flash 75L The product containing fractions the solvent is removed by rotary evaporation The product is dried under vacuum at 100° C. yielding a white crystalline solid
来源 ID: ord-f8cea3afce68461aa3ed3ff4ad81ec87反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of 3-(Benzylamino)-1,1,1-trifluoropropan-2-ol (2.68 g, 12.3 mmol) and triethylamine (1.7 mL, 12.2 mmol) in CH2Cl2 is cooled to 0° C. The solution is treated drop wise with 2-bromopropanoyl chloride (1.2 mL, 12 mmol, Aldrich) and stirred for 5 minutes. The solution is diluted to 100 mL with CH2Cl2 and washed sequentially with 1.0 M HCl, saturated NaHCO3, and brine (100 mL each). The organic layer is dried over Na2SO4 and filtered. The solvent is removed by rotary evaporation yielding (N-benzyl-2-bromo-N-(3,3,3-trifluoro-2-hydroxypropyl)propanamide as a golden oil. Dry NaH is suspended in dry, inhibitor free THF (25 ml) in a flame dried flask and the mixture is cooled to 0° C. with stirring on an ice bath. The N-benzyl-2-bromo-N-(3,3,3-trifluoro-2-hydroxypropyl)propanamide (4.25 g, 12 mmol) is added as a solution in dry, inhibitor free THF (25 ml) and the resultant suspension is warmed to RT. After stirring for one hour the reaction is quenched with MeOH over an ice bath until no more gas evolved and the mixture is poured into 1.0 M HCl (200 mL). The aqueous mixture is extracted into MTBE (200 mL) and the organic layer is washed with saturated NaHCO3 and brine (200 mL each). The organic layer is dried over Na2SO4 and filtered, and the solvent is removed by rotary evaporation yielding an amber oil. washed sequentially with 1.0 M HCl, saturated NaHCO3, and brine (100 mL each) The organic layer is dried over Na2SO4 filtered The solvent is removed by rotary evaporation
来源 ID: ord-f9074aa483654f5182bf1394114d6fa2反应条件: temp:-10.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Lithium triflate was suspended in CH3CN (15 mL) and the mixture is cooled to −10° C. 2-(Trifluoromethyl)oxirane is added and the suspension is allowed to warm to RT with stirring. Benzylamine (6.33 mL, 58 mmol, Aldrich) is added all-at-once and the resultant solution is stirred for 25 minutes. The reaction is quenched by pouring into CH2Cl2 (200 mL) and washing 3× with H2O (200 mL). The organic layer is dried over Na2SO4 and filtered. The product is purified on a Biotage Flash 75L using 20:70:10 CH2Cl2:pentane:triethylamine as eluent. The product containing fractions are pooled and the solvent is removed by rotary evaporation. The product is dried under vacuum at 100° C. yielding a white crystalline solid. to warm to RT is stirred for 25 minutes The reaction is quenched by pouring into CH2Cl2 (200 mL) washing 3× with H2O (200 mL) The organic layer is dried over Na2SO4 filtered The product is purified on a Biotage Flash 75L The product containing fractions the solvent is removed by rotary evaporation The product is dried under vacuum at 100° C. yielding a white crystalline solid
来源 ID: ord-087e9a7eb0cb46e1883054e14dfd2956反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of 3-(Benzylamino)-1,1,1-trifluoropropan-2-ol (2.68 g, 12.3 mmol) and triethylamine (1.7 mL, 12.2 mmol) in CH2Cl2 is cooled to 0° C. The solution is treated drop wise with 2-bromopropanoyl chloride (1.2 mL, 12 mmol, Aldrich) and stirred for 5 minutes. The solution is diluted to 100 mL with CH2Cl2 and washed sequentially with 1.0M HCl, saturated NaHCO3, and brine (100 mL each). The organic layer is dried over Na2SO4 and filtered. The solvent is removed by rotary evaporation yielding (N-benzyl-2-bromo-N-(3,3,3-trifluoro-2-hydroxypropyl)propanamide as a golden oil. Dry NaH is suspended in dry, inhibitor free THF (25 ml) in a flame dried flask and the mixture is cooled to 0° C. with stirring on an ice bath. The N-benzyl-2-bromo-N-(3,3,3-trifluoro-2-hydroxypropyl)propanamide (4.25 g, 12 mmol) is added as a solution in dry, inhibitor free THF (25 ml) and the resultant suspension is warmed to RT. After stirring for one hour the reaction is quenched with MeOH over an ice bath until no more gas evolved and the mixture is poured into 1.0M HCl (200 mL). The aqueous mixture is extracted into MTBE (200 mL) and the organic layer is washed with saturated NaHCO3 and brine (200 mL each). The organic layer is dried over Na2SO4 and filtered, and the solvent is removed by rotary evaporation yielding an amber oil. washed sequentially with 1.0M HCl, saturated NaHCO3, and brine (100 mL each) The organic layer is dried over Na2SO4 filtered The solvent is removed by rotary evaporation
来源 ID: ord-5f44b8791b2d45f7b5753f3f56fda1b8反应条件: temp:-10.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Lithium triflate was suspended in CH3CN (15 mL) and the mixture is cooled to −10° C. 2-(Trifluoromethyl)oxirane is added and the suspension is allowed to warm to RT with stirring. Benzylamine (6.33 mL, 58 mmol, Aldrich) is added all-at-once and the resultant solution is stirred for 25 minutes. The reaction is quenched by pouring into CH2Cl2 (200 mL) and washing 3× with H2O (200 mL). The organic layer is dried over Na2SO4 and filtered. The product is purified on a Biotage Flash 75L using 20:70:10 CH2Cl2:pentane:triethylamine as eluent. The product containing fractions are pooled and the solvent is removed by rotary evaporation. The product is dried under vacuum at 100° C. yielding a white crystalline solid. to warm to RT is stirred for 25 minutes The reaction is quenched by pouring into CH2Cl2 (200 mL) washing 3× with H2O (200 mL) The organic layer is dried over Na2SO4 filtered The product is purified on a Biotage Flash 75L The product containing fractions the solvent is removed by rotary evaporation The product is dried under vacuum at 100° C. yielding a white crystalline solid
来源 ID: ord-ec22d8c9036b4771b17deb1b36346f0e反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Starting material: benzylamine and 2-(trifluoromethyl)oxirane
来源 ID: ord-1462ed97ac0c4e36bccc605e1b15eb07PubChem References
以下资料来自该化合物的公开数据库参考记录。