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HRID 248845作成日:2026年10月26日

Thionyl Chloride → N-benzyl-2-chloro-N-methylethanamine

https://huagongshe.com/reaction/248845

反応式

関与物質

役割名称HCID仕込み量
反応物Thionyl ChlorideHCID 24386—
反応物N-Benzyl-N-methylethanolamineHCID 66876—
触媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物N-benzyl-2-chloro-N-methylethanamineHCID 3196879.1%

反応手順

33 g of N-benzyl-N-methyl-2-aminoethanol were dissolved in 300 ml of dichloromethane. 48 g of thionyl chloride and 2 drops of dimethylformamide were added to the solution at 0° C. The reaction mixture was then heated under reflux for 6 hours. The reaction mixture was worked up by evaporating it to dryness and taking up the residue three times in 300 ml portions of toluene and again evaporating to dryness. The remaining residue was dissolved in dichloromethane and the N-benzyl-N-(2-chloroethyl)-N-methylamine hydrochloride was crystallized by addition of diethyl ether to the solution. The crystals (m.p. 142° C.-145° C.) were filtered out and dissolved in ice water. The solution was adjusted to alkaline pH 9 by addition of aqueous sodium hydroxide solution and then extracted with toluene. The organic phase was separated, dried over sodium sulfate, filtered and concentrated under reduced pressure. 29 g of N-benzyl-N-(2- chloroethyl)-N-methylamine were obtained as a residue.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05212173
出典データセットuspto-grants-1993_05
ORD IDord-ab2537e535ec47f8af68b8af48329d29
出典メモuspto-grants-1993_05