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4-Bromothiophenol → 1-Bromo-4-cyclopropylthiobenzene

HRID 1039506
ノート
印刷プレビュー

反応式

HRID 1039506 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 660494-BromothiophenolHCID 78037BromocyclopropaneHCID 23665647Potassium tert-butoxide

生成物 1

HCID 223501051-Bromo-4-cyclopropylthiobenzene

試薬・触媒・溶媒 2

HCID 679Dimethyl Sulfoxide溶媒HCID 3283Diethyl Ether溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-602a16a27a1c4b6aa8bc217742b9df7b
出典データセット
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08551993B2

反応ノート

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