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Dimethyl Disulfide → [2-(4-Methyl-5-thiazolyl)ethyl]-methyl-disulphide

HRID 66065
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인쇄 미리보기

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HRID 66065 반응식
[CH3:1][C:2]1[N:3]=[CH:4][S:5][C:6]=1[CH2:7][CH2:8][SH:9].[CH3:10][S:11]SC>[H-].[Na+]>[CH3:1][C:2]1[N:3]=[CH:4][S:5][C:6]=1[CH2:7][CH2:8][S:9][S:11][CH3:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 12232Dimethyl DisulfideHCID 186900032-(4-Methyl-1,3-thiazol-5-yl)ethane-1-thiol

생성물 1

HCID 20306425[2-(4-Methyl-5-thiazolyl)ethyl]-methyl-disulphide수율 60.4%

시약·촉매·용매 1

HCID 24758Sodium hydride촉매

실험 절차

A mixture of 8.26 g (0.052 mol) of 2-(4-methyl-5-thiazolyl)-ethyl-mercaptan and 33.07 g (0.208 mol) of dimethyldisulphide is treated with 50 mg of sodium hydride (50% dispersion in oil) and the mixture is heated to reflux for 4 hours. The mixture is then left to cool, filtered over 10 g of aluminium oxide (activity I, neutral), which is back-washed with ether, and concentrated in a vacuum. The resulting crude product (9.5 g) is distilled through a Hempel column under a high vacuum, there being obtained 6.45 g of [2-(4-methyl-5-thiazolyl)-ethyl]-methyl-disulphide. Boiling point 104°-110°/0.02 mm Hg; nD20 = 1.5944; purity: 99%. IR (liq.): bands inter alia at 3100, 2960, 1545, 1415, 1220, 955, 1005, 840, 795 cm-1.

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후처리

  1. temperaturethe mixture is heated
  2. temperatureto reflux for 4 hours
  3. waitThe mixture is then left
  4. temperatureto cool
  5. filtrationfiltered over 10 g of aluminium oxide (activity I, neutral), which
  6. washis back-washed with ether
  7. concentrationconcentrated in a vacuum
  8. distillationThe resulting crude product (9.5 g) is distilled through a Hempel column under a high vacuum

출처 및 근거

ORD 기록
ord-f5cb927177a041298154da5508183217
출처 데이터셋
uspto-grants-1978_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04130562

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