Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 3762생성일: 2026년 10월 23일
Quinuclidine, 3-amino-, dihydrochloride → N-(1-Azabicyclo[2.2.2]oct-3-yl)-2-propoxybenzamide hydrochloride
https://huagongshe.com/ko/reaction/3762
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Quinuclidine, 3-amino-, dihydrochloride | HCID 197853 | — |
| 반응물 | 2-Propoxybenzoyl chloride | HCID 15921913 | — |
| 반응물 | Barium hydroxide, octahydrate | HCID 17749109 | — |
| 용매 | Carbon Dioxide | HCID 280 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | N-(1-Azabicyclo[2.2.2]oct-3-yl)-2-propoxybenzamide hydrochloride | HCID 13630995 | — |
반응 단계
To a solution of 3.82 g (0.0192 mole) of 3-amino quinuclidine dihydrochloride in about 25 ml of carbon dioxide-free water was added 8 g (0.025 mole) of barium hydroxide octahydrate. The mixture was warmed for 5 minutes and then dried to a powder on a rotary evaporator. While protecting from contamination with carbon dioxide in the atmosphere, the powder was extracted in sequence with hot benzene and a 1:1 mixture of benzene-methylene chloride solution. The combined extracts were dried over magnesium sulfate and the mixture filtered. To the filtrate with agitation was added dropwise a solution of 3.4 g (0.0171 mole) of 2-propoxybenzoyl chloride in 50 ml of methylene chloride. The mixture was warmed on a steam bath to evaporate about 75% of the methylene chloride. Ligroin (60-110) was added and the mixture solidified. The solid was recrystallized from anhydrous ethyl alcohol to give 3.9 g (62.0%), m.p. 210°-211° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04722834 |
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| 출처 데이터셋 | uspto-grants-1988_02 |
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| ORD ID | ord-03d1b8f05e4141739d0b6c4cac54a2f6 |
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| 출처 메모 | uspto-grants-1988_02 |
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