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4-Bromothiophenol → 1-Bromo-4-cyclopropylthiobenzene

HRID 1039506
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HRID 1039506 반응식
[CH3:1][C:2]([CH3:5])([O-])C.[K+].[Br:7][C:8]1[CH:13]=[CH:12][C:11]([SH:14])=[CH:10][CH:9]=1.BrC1CC1>CS(C)=O.CCOCC>[Br:7][C:8]1[CH:13]=[CH:12][C:11]([S:14][CH:5]2[CH2:2][CH2:1]2)=[CH:10][CH:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 660494-BromothiophenolHCID 78037BromocyclopropaneHCID 23665647Potassium tert-butoxide

생성물 1

HCID 223501051-Bromo-4-cyclopropylthiobenzene

시약·촉매·용매 2

HCID 679Dimethyl Sulfoxide용매HCID 3283Diethyl Ether용매

실험 절차

To a degassed solution of potassium tert-butoxide (2.08 g, 18.51 mmol) in dry dimethylsulphoxide (6 mL), 4-bromo-benzenethiol (3.5 g, 18.5 mmol) was added and the mixture was stirred for 15 min at ambient temperature under nitrogen. Bromocyclopropane (4.4 mL, 55.5 mmol) was added afterwards and the reaction mixture was heated at 80° C. for 24 h in a sealed vessel. The mixture was cooled, diluted with ether (150 mL) and washed with water (100 mL). The aqueous layer was extracted with ether (3×50 mL). Combined organic extracts were finally dried with anhydrous magnesium sulfate. 1-Bromo-4-cyclopropylsulfanyl-benzene was obtained after evaporation of the solvent as yellow liquid.

후처리

  1. temperaturethe reaction mixture was heated at 80° C. for 24 h in a sealed vessel
  2. temperatureThe mixture was cooled
  3. washwashed with water (100 mL)
  4. extractionThe aqueous layer was extracted with ether (3×50 mL)
  5. dry with materialCombined organic extracts were finally dried with anhydrous magnesium sulfate

출처 및 근거

ORD 기록
ord-602a16a27a1c4b6aa8bc217742b9df7b
출처 데이터셋
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08551993B2

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