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Benzenesulfenyl chloride → 2-p-Anisyl-5-(phenylthio)thiophene

HRID 46651
노트
인쇄 미리보기

반응식

HRID 46651 반응식
[CH2:1]([C:10]1[S:11][CH:12]=[CH:13][CH:14]=1)[C:2]1[CH:7]=[CH:6][C:5]([O:8][CH3:9])=[CH:4][CH:3]=1.[C:15]1([S:21]Cl)[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1>C(Cl)(Cl)(Cl)Cl.[Fe]>[CH2:1]([C:10]1[S:11][C:12]([S:21][C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)=[CH:13][CH:14]=1)[C:2]1[CH:3]=[CH:4][C:5]([O:8][CH3:9])=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 11008040Benzenesulfenyl chlorideHCID 110309412-(4-Methoxybenzyl)thiophene

생성물 1

HCID 203866452-p-Anisyl-5-(phenylthio)thiophene수율 29%

시약·촉매·용매 2

HCID 23925Iron촉매HCID 5943Carbon Tetrachloride용매

실험 절차

A solution of 34 g (0.179 mole) of 2-p-anisylthiophene in 500 ml of carbon tetrachloride was treated with 23 ml (28.5 g, 0.197 mole) of benzenesulfenyl chloride and 0.1 g of iron powder. The mixture was allowed to stand at room temperature for eight days. The mixture was filtered to remove a small amount of solid. The filtrate was evaporated to give 67 g of crude solid product. Recrystallization from 220 ml of ethyl acetate gave 15.4 g (29%) of 2-p-anisyl-5-(phenylthio)thiophene, m.p. 92°-93° C.

후처리

  1. filtrationThe mixture was filtered
  2. customto remove a small amount of solid
  3. customThe filtrate was evaporated
  4. customto give 67 g of crude solid product
  5. customRecrystallization from 220 ml of ethyl acetate

출처 및 근거

ORD 기록
ord-b702cd1924054e6f97e089e9f9f5781a
출처 데이터셋
uspto-grants-1979_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04174405

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