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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1648626생성일: 2026년 10월 26일

Dichloromethane → (E)-3-Chloro-N-(6,6-dimethyl-2-hepten-4-ynyl)-N-methylbenzo[b]thiophene-7-methanamine hydrochloride

https://huagongshe.com/reaction/1648626

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물Potassium CarbonateHCID 11430—
반응물7-(Bromomethyl)-3-chloro-1-benzothiopheneHCID 14780520—
반응물(E)-N-methyl-6,6-dimethyl-2-hepten-4-ynylamine hydrochlorideHCID 19917487—
용매Dimethyl SulfoxideHCID 679—
생성물(E)-3-Chloro-N-(6,6-dimethyl-2-hepten-4-ynyl)-N-methylbenzo[b]thiophene-7-methanamine hydrochlorideHCID 691806977%

반응 단계

To a solution of 0.34 g (1.3 mmol) of 7-bromomethyl-3-chiorobenzo[b]thiophene in 3 ml of dimethyl sulfoxide were added 0.246 g (1.31 mmol) of (E)-N-(6,6-dimethyl-2-hepten-4-ynyl)methyiamine hydrochloride, and 0.27 g (1.95 mmol) of potassium carbonate under ice cooling. The mixture was stirred for 19 hours at room temperature, poured into 40 ml of dichioromethane, washed with 30 ml ×2 of water, and adjusted to pH 2 with 25 ml of water and 2N hydrochloric acid. The organic layer was separated washed with 20 ml of saturated sodium chloride aqueous solution, dried over anhydrous magnesium sulfate, concentrated under reduced pressure and cooled to crystallize. The crystals were suspended in isopropylalcohol, filtered, washed with isopropyl alcohol and dried to obtain 0.37 g (yield: 77%) of the above identified compound as white crystalline powder.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05436354
출처 데이터셋uspto-grants-1995_07
ORD IDord-38916b635529447ea33d446f863dc0a0
출처 메모uspto-grants-1995_07