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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 892786생성일: 2026년 10월 25일

Triethylamine → 2-(Dimethylamino)methyl-3-methylthiophene

https://huagongshe.com/reaction/892786

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Thionyl ChlorideHCID 24386—
반응물(3-Methylthiophen-2-yl)methanolHCID 12875263—
용매DichloromethaneHCID 6344—
생성물2-(Dimethylamino)methyl-3-methylthiopheneHCID 1008066875%

반응 단계

In 200 ml of methylene chloride were dissolved 20.8 g of 3-methyl-2-thenyl alcohol and 27.1 ml of triethylamine, and 12.9 ml of thionyl chloride was added thereto dropwise at -15° C. to -10° C. over a period of 30 minutes, after which the resulting solution was further subjected to reaction at the same temperature for 30 minutes. The reaction mixture was poured into ice water, and the organic layer was separated and then dried over anhydrous magnesium sulfate. Subsequently, the dried organic layer was added dropwise with ice-cooling to a solution of 95 g of dimethylamine in 550 ml of ethanol, and the resulting mixture was allowed to stand overnight at room temperature. The solvent was removed by distillation under reduced pressure, after which 100 ml of water was added to the residue, and the resulting mixture was adjusted to pH 10 with potassium carbonate, and then extracted with 200 ml of ethyl acetate. The extract was washed with 50 ml of a saturated aqueous sodium chloride solution and dried over anhydrous potassium carbonate, after which the solvent was removed by distillation under reduced pressure, and the oily substance thus obtained was distilled under reduced pressure to obtain 19.0 g (yield 75%) of 2-(dimethylamino)methyl-3-methylthiophene having a boiling point of 85°-86° C./14 mmHg.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05120746
출처 데이터셋uspto-grants-1992_06
ORD IDord-b916c9ed0a8f47f9816ec22076886cf8
출처 메모uspto-grants-1992_06