Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 487791생성일: 2026년 10월 25일
Dichloromethane → (E)-3-Chloro-N-(6,6-dimethyl-2-hepten-4-ynyl)-N-methylbenzo[b]thiophene-7-methanamine hydrochloride
https://huagongshe.com/reaction/487791
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dichloromethane | HCID 6344 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 7-(Bromomethyl)-3-chloro-1-benzothiophene | HCID 14780520 | — |
| 반응물 | (E)-N-methyl-6,6-dimethyl-2-hepten-4-ynylamine hydrochloride | HCID 19917487 | — |
| 용매 | Dimethyl Sulfoxide | HCID 679 | — |
| 생성물 | (E)-3-Chloro-N-(6,6-dimethyl-2-hepten-4-ynyl)-N-methylbenzo[b]thiophene-7-methanamine hydrochloride | HCID 6918069 | 77% |
반응 단계
To a solution of 0.34 g (1.3 mmol) of 7-bromomethyl3-chlorobenzo[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)methylamine 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 dichloromethane, 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05296612 |
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| 출처 데이터셋 | uspto-grants-1994_03 |
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| ORD ID | ord-9ebe147267ee44378620a10e05f4e327 |
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| 출처 메모 | uspto-grants-1994_03 |
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