反应 #4146120
相关文献 (1)
openreactiondata ↗doi:10.1039/C8SC04228D
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-b057229743b44db28513887affda222c暂无可渲染的结构数据
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2-氟乙醇(CAS 371-62-0)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:
来源 ID: ord-b057229743b44db28513887affda222c反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-7e90660afbe64de8a4c39446e6fc5814反应条件: temp:0.00; pressure:0.00; stir:
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来源 ID: ord-27c8da0bba644221a446d1ce7a6a2f16反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-1d422825230844a8957c37e583857c2d反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-6e7ff9c56bff4525a08321161a02443b反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-7a96dda3681440a19a558dced8445007反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-c4979e58209a44808f1e214ede8a7a5c反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-a8532651421c47ce92f33d7ba270ddf7反应条件: temp:60.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: KHMDS (0.320 g, 1.60 mmol) is added to an ice-cooled mixture of N-(4-fluoro-3-chloro-phenyl)-2-fluoro-4-methylamino-5-nitro-benzoic acid amide (500 mg, 1.46 mmol), 2-fluoroethanol (0.129 ml, 2.19 mmol) and 30 ml THF. After 30 min the temperature is raised to 60° C. for 4.5 h, then it is stirred at rt overnight. Additional 2-fluoroethanol (0.129 ml, 2.19 mmol) and KHMDS (0.160 g, 0.80 mmol) are added and it is stirred for 4.5 h at 60° C. Then the mixture is diluted with satd. aq. NaHCO3-solution and the precipitate is filtered off, washed with water and dried. cooled it is stirred for 4.5 h at 60° C Then the mixture is diluted with satd aq. NaHCO3-solution and the precipitate is filtered off washed with water dried
来源 ID: ord-4a986c4676314b6fb8251efc18976a08反应条件: temp:1020.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of 2-fluoroethanol (3.2 g, 50 mmol) and triethylamine (5.5 g, 55 mmol) in dichloromethane (60 mL) was added dropwise (CF3SO2)2O (15.5 g, 55 mmol) at −78° C. under N2. The mixture was stirred at 1020° C. for 1 h, and treated with water (100 mL). The organic layer was washed with satd aq NaHCO3 (100 mL) and brine (100 mL), dried, and concentrated to give 2-fluoroethyl trifluoromethanesulfonate (8 g, yield 82%). The organic layer was washed with satd aq NaHCO3 (100 mL) and brine (100 mL) dried concentrated
来源 ID: ord-2eaedce07b0e4428b1de8dcf6e53c090PubChem References
以下资料来自该化合物的公开数据库参考记录。
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