Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1249037생성일: 2026년 10월 26일
Ethanol → (3R)-2-[(Benzylthio)thiocarbonyl]-1,2,3,4-tetrahydro-beta-carboline-3-carboxylic acid
https://huagongshe.com/reaction/1249037
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethanol | HCID 702 | — |
| 반응물 | Carbon Disulfide | HCID 6348 | — |
| 반응물 | Benzyl Bromide | HCID 7498 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | D-1,2,3,4-Tetrahydronorharman-3-carboxylic acid | HCID 675102 | — |
| 생성물 | (3R)-2-[(Benzylthio)thiocarbonyl]-1,2,3,4-tetrahydro-beta-carboline-3-carboxylic acid | HCID 13561931 | — |
반응 단계
To a mixture of (3R)-1,2,3,4-tetrahydro-β-carboline-3-carboxylic acid (5.4 g), 2N NaOH (25 ml) and 50% ethanol (70 ml) is added dropwise carbon disulfide (1.5 ml) at room temperature. The mixture is stirred at room temperature for 30 minutes, and thereto is added dropwise benzyl bromide (3.5 ml), and the mixture is further stirred at the same temperature for 3 hours and then distilled to remover the solvent. To the residue is added water, and the mixture is extracted with ether. The aqueous layer is acidified with 10% HCl, extracted with ethyl acetate. The extract is washed with water, dried and distilled to remove the solvent. The residue is purified by silica gel column chromatography (solvent, chloroform:methanol=20:1) to give the title compound (4.5 g) as pale yellow powder.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04628057 |
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| 출처 데이터셋 | uspto-grants-1986_12 |
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| ORD ID | ord-0271a25bd06d4969a382bfb50786e4d6 |
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| 출처 메모 | uspto-grants-1986_12 |
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