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Hydrogen Sulfide → 3-Hydroxy-3-mercaptomethylquinuclidine

HRID 2098311
ノート
印刷プレビュー

反応式

HRID 2098311 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 402Hydrogen SulfideHCID 887Methanol2 回HCID 1408933-Methylenequinuclidine2 回

生成物 1

HCID 111267633-Hydroxy-3-mercaptomethylquinuclidine

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

実験手順

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.

後処理

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

出典と根拠

ORDレコード
ord-32287a4d09074ebb92685fcfe658edc8
出典データセット
uspto-grants-2013_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08450487B2

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート