反応 #4118489
関連文献 (1)
openreactiondata ↗doi:10.1039/C8SC04228D
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-d637ebf259d1456eb4da6842146c1dd0表示可能な構造データがありません
CCS(=O)(=O)CCCl製品情報
1-chloro-2-ethylsulfonylethane (CAS 25027-40-1) product identity, structure identifiers and related reaction data for chemical intermediate research and sourcing review.
想定用途
専門的研究・工業用途限定
データベース ID 101406
安全上の注意
For professional research and industrial use only. Review the supplier safety data sheet before handling.
合成データ
12 反応 · 12 文献
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-d637ebf259d1456eb4da6842146c1dd0反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-504c7758faa24d7bb5e7071dcb179bc8反応条件: temp:50.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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
ソース ID: ord-7ed1fbeb69b444819da3f0b8709dc87d反応条件: temp:50.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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
ソース ID: ord-7ed1fbeb69b444819da3f0b8709dc87d反応条件: temp:50.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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
ソース ID: ord-b546acbb437146d58bfdb310fbcc1266反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-d637ebf259d1456eb4da6842146c1dd0反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-504c7758faa24d7bb5e7071dcb179bc8反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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
ソース ID: ord-979d9525aacd48d9906aa36270522784反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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
ソース ID: ord-979d9525aacd48d9906aa36270522784反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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
ソース ID: ord-979d9525aacd48d9906aa36270522784反応条件: temp:50.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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
ソース ID: ord-7ed1fbeb69b444819da3f0b8709dc87d反応条件: temp:50.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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
ソース ID: ord-b546acbb437146d58bfdb310fbcc1266PubChem References
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