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Benzyl mercaptan → 4-(Benzylsulfanyl)-1,3-thiazole

HRID 2073693
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HRID 2073693 반응식
[CH2:1]([SH:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C[O-].[Na+].Cl[C:13]1[N:14]=[CH:15][S:16][CH:17]=1>C(O)C>[C:2]1([CH2:1][S:8][C:13]2[N:14]=[CH:15][S:16][CH:17]=2)[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
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참가 물질

5

반응물 3

HCID 7509Benzyl mercaptanHCID 10942334Sodium MethoxideHCID 135173944-Chloro-1,3-thiazole

생성물 1

HCID 150771204-(Benzylsulfanyl)-1,3-thiazole수율 37.8%

시약·촉매·용매 1

HCID 702Ethanol용매2회

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온도
65 °C

실험 절차

Benzylmercaptan (24.8 g) was added slowly to a solution of 10.8 g of sodium methoxide in 100 ml ethanol. After 10 minutes, the reaction mixture was heated to 65° C. and a solution of 23.8 g of 4-chlorothiazole [prepared by the method of P. Reynaud et al., Bull. Soc. Chim. France, 1735 (1962)] in 25 ml ethanol was added dropwise. When addition was complete, the reaction mixture was refluxed 36 hours. The reaction mixture was cooled, and the bulk of the solvent evaporated. Cold water (300 ml) was added to the residue, and the aqueous mixture was extracted with 200 ml ether followed by 200 ml methylene chloride. The combined organic solution was washed with brine, dried over magnesium sulfate, filtered and the solvent evaporated. Distillation of the resulting yellow oil gave 15.6 g of 4-(phenylmethylthio)thiazole, bp 122-134 (0.6 mm).

후처리

  1. additionWhen addition
  2. temperaturethe reaction mixture was refluxed 36 hours
  3. temperatureThe reaction mixture was cooled
  4. customthe bulk of the solvent evaporated
  5. additionCold water (300 ml) was added to the residue
  6. extractionthe aqueous mixture was extracted with 200 ml ether
  7. washThe combined organic solution was washed with brine
  8. dry with materialdried over magnesium sulfate
  9. filtrationfiltered
  10. customthe solvent evaporated
  11. distillationDistillation of the resulting yellow oil

출처 및 근거

ORD 기록
ord-bbed34baa8114ff89f3a5ec24279a3aa
출처 데이터셋
uspto-grants-1990_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04919706

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