反应 #4118489
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-d637ebf259d1456eb4da6842146c1dd0暂无可渲染的结构数据
CCS(=O)(=O)CCCl产品信息
1-氯-2-(乙基磺酰基)乙烷(CAS 25027-40-1)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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合成路线数据
12 条反应 · 12 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-d637ebf259d1456eb4da6842146c1dd0反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-504c7758faa24d7bb5e7071dcb179bc8反应条件: temp:50.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Gaseous methylamine is passed to saturation (about 30 min) into a solution of 15.7 g of chloroethyl ethyl sulfone in 100 ml of toluene at an internal temperature of 50° C. The mixture is stirred at 50° C. for 3 h, the precipitate is filtered off with suction, and the filtrate is concentrated in a rotary evaporator. The remaining yellow mobile liquid (12.3 g) is reacted without further purification. the precipitate is filtered off with suction the filtrate is concentrated in a rotary evaporator The remaining yellow mobile liquid (12.3 g) is reacted without further purification
来源 ID: ord-7ed1fbeb69b444819da3f0b8709dc87d反应条件: temp:50.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Gaseous methylamine is passed to saturation (about 30 min) into a solution of 15.7 g of chloroethyl ethyl sulfone in 100 ml of toluene at an internal temperature of 50° C. The mixture is stirred at 50° C. for 3 h, the precipitate is filtered off with suction, and the filtrate is concentrated in a rotary evaporator. The remaining yellow mobile liquid (12.3 g) is reacted without further purification. the precipitate is filtered off with suction the filtrate is concentrated in a rotary evaporator The remaining yellow mobile liquid (12.3 g) is reacted without further purification
来源 ID: ord-7ed1fbeb69b444819da3f0b8709dc87d反应条件: temp:50.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of 15.7 g of chloroethyl ethyl sulfone in 50 ml of toluene is added dropwise within 10 min to a solution of 73 g of n-butylamine and 10.1 g of triethylamine in 100 ml of toluene at an internal temperature of 50° C. The mixture is stirred at 50° C. for 5 h and allowed to cool to room temperature, the precipitate is filtered off with suction, and the filtrate is concentrated in a rotary evaporator. The remaining yellow oil (18.7 g) is reacted without further purification. to cool to room temperature the precipitate is filtered off with suction the filtrate is concentrated in a rotary evaporator The remaining yellow oil (18.7 g) is reacted without further purification
来源 ID: ord-b546acbb437146d58bfdb310fbcc1266反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-d637ebf259d1456eb4da6842146c1dd0反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-504c7758faa24d7bb5e7071dcb179bc8反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Mix 2-chloroethyl ethyl sulfone (1.2 g, 7.66 mmol) and piperidine (2 mL, 20 mmol). Stir at room temperature for 2 hours. Treat with 5N sodium hydroxide, extract with ethyl acetate (3×50 mL) and dry (MgSO4). Concentrate in vacuo to yield 1.3 g yellow oil which crystallizes. Purify by silica gel chromatography (ethyl acetate) to yield 550 mg (35%) of the title compound as a clear oil which crystallizes; mp 45°-47° C. extract with ethyl acetate (3×50 mL) dry (MgSO4) Concentrate in vacuo
来源 ID: ord-979d9525aacd48d9906aa36270522784反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Mix 2-chloroethyl ethyl sulfone (1.2 g, 7.66 mmol) and piperidine (2 mL, 20 mmol). Stir at room temperature for 2 hours. Treat with 5N sodium hydroxide, extract with ethyl acetate (3×50 mL) and dry (MgSO4). Concentrate in vacuo to yield 1.3 g yellow oil which crystallizes. Purify by silica gel chromatography (ethyl acetate) to yield 550 mg (35%) of the title compound as a clear oil which crystallizes; mp 45°-47° C. extract with ethyl acetate (3×50 mL) dry (MgSO4) Concentrate in vacuo
来源 ID: ord-979d9525aacd48d9906aa36270522784反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Mix 2-chloroethyl ethyl sulfone (1.2 g, 7.66 mmol) and piperidine (2 mL, 20 mmol). Stir at room temperature for 2 hours. Treat with 5N sodium hydroxide, extract with ethyl acetate (3×50 mL) and dry (MgSO4). Concentrate in vacuo to yield 1.3 g yellow oil which crystallizes. Purify by silica gel chromatography (ethyl acetate) to yield 550 mg (35%) of the title compound as a clear oil which crystallizes; mp 45°-47° C. extract with ethyl acetate (3×50 mL) dry (MgSO4) Concentrate in vacuo
来源 ID: ord-979d9525aacd48d9906aa36270522784反应条件: temp:50.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Gaseous methylamine is passed to saturation (about 30 min) into a solution of 15.7 g of chloroethyl ethyl sulfone in 100 ml of toluene at an internal temperature of 50° C. The mixture is stirred at 50° C. for 3 h, the precipitate is filtered off with suction, and the filtrate is concentrated in a rotary evaporator. The remaining yellow mobile liquid (12.3 g) is reacted without further purification. the precipitate is filtered off with suction the filtrate is concentrated in a rotary evaporator The remaining yellow mobile liquid (12.3 g) is reacted without further purification
来源 ID: ord-7ed1fbeb69b444819da3f0b8709dc87d反应条件: temp:50.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of 15.7 g of chloroethyl ethyl sulfone in 50 ml of toluene is added dropwise within 10 min to a solution of 73 g of n-butylamine and 10.1 g of triethylamine in 100 ml of toluene at an internal temperature of 50° C. The mixture is stirred at 50° C. for 5 h and allowed to cool to room temperature, the precipitate is filtered off with suction, and the filtrate is concentrated in a rotary evaporator. The remaining yellow oil (18.7 g) is reacted without further purification. to cool to room temperature the precipitate is filtered off with suction the filtrate is concentrated in a rotary evaporator The remaining yellow oil (18.7 g) is reacted without further purification
来源 ID: ord-b546acbb437146d58bfdb310fbcc1266PubChem References
以下资料来自该化合物的公开数据库参考记录。
