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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrogen Sulfide → 3-Hydroxy-3-mercaptomethylquinuclidine

HRID 2098311
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HRID 2098311 반응식
[CH2:1]=[C:2]1[CH:7]2[CH2:8][CH2:9][N:4]([CH2:5][CH2:6]2)[CH2:3]1.[SH2:10].C[OH:12]>ClCCl>[OH:12][C:2]1([CH2:1][SH:10])[CH:7]2[CH2:8][CH2:9][N:4]([CH2:5][CH2:6]2)[CH2:3]1
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참가 물질

5

반응물 3

HCID 402Hydrogen SulfideHCID 887Methanol2회HCID 1408933-Methylenequinuclidine2회

생성물 1

HCID 111267633-Hydroxy-3-mercaptomethylquinuclidine

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

A solution of the epoxide of 3-methylene quinuclidine (100 g, 0.719 moles) in dichloromethane was cooled to a temperature between about 0 to 5° C. The solution was charged with methanol (100 ml). The mass was stirred for 10 to 15 minutes at this temperature range. To this cold solution hydrogen sulfide gas (50 g, 1.4 mol) was passed and after the passing was complete, the reaction was continued at this temperature for 2 to 3 hours, monitored by gas chromatography, whereupon the peak of epoxide of 3-methylene quinuclidine disappeared. After completion of the reaction, a dichloromethane solution of 3-hydroxy 3-mecapto methylquinuclidine in methanol was obtained. This solution was used for the next step.

후처리

  1. waitthe reaction was continued at this temperature for 2 to 3 hours
  2. customAfter completion of the reaction

출처 및 근거

ORD 기록
ord-32287a4d09074ebb92685fcfe658edc8
출처 데이터셋
uspto-grants-2013_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08450487B2

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