Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1732569생성일: 2026년 10월 26일
4-Hydroxybenzaldehyde → Methyl 1-(4-hydroxybenzyl)-1,2,5,6-tetrahydropyridine-3-carboxylate hydrochloride
https://huagongshe.com/reaction/1732569
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 4-Hydroxybenzaldehyde | HCID 126 | — |
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Norarecoline Hydrochloride | HCID 201540 | — |
| 반응물 | Sodium cyanoborohydride | HCID 5003444 | — |
| 용매 | Acetone | HCID 180 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | Methyl 1-(4-hydroxybenzyl)-1,2,5,6-tetrahydropyridine-3-carboxylate hydrochloride | HCID 12769335 | 65.8% |
반응 단계
4-Hydroxybenzaldehyde (1.34 g.) and sodium cyanoborohydride (0.7 g.) were added to a solution of methyl 1,2,5,6-tetrahydropyridine-3-carboxylate hydrochloride (3.1 g.) in methanol (30 ml.). The mixture was stirred for 3 days at 25° C., evaporated and water (30 ml.) added to the residue followed by concentrated hydrochloric acid to pH 1. This mixture was extracted with ether (2×20 ml.) and the extracts discarded. The aqueous phase was basified to pH 9 with 10% w/v sodium carbonate solution and then extracted with ether (2×30 ml.). The combined extracts were dried (MgSO4) and evaporated. The oil obtained was dissolved in acetone and treated with a slight excess of ethereal hydrogen chloride. The solid which was precipitated was collected by filtration to give methyl 1-(4-hydroxybenzyl)-1,2,5,6-tetrahydropyridine-3-carboxylate hydrochloride (2.05 g.). A portion was recrystallised from methanol and acetone to give pure material of m.p. 212°-214° C. (dec.).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US04238488 |
|---|
| 출처 데이터셋 | uspto-grants-1980_12 |
|---|
| ORD ID | ord-e8a43c1ee1a544ec971435893d5c4d7b |
|---|
| 출처 메모 | uspto-grants-1980_12 |
|---|