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Water → (4-Bromo-3-(difluoromethyl)phenyl)(ethyl)sulfane

HRID 1846032
ノート
印刷プレビュー

反応式

HRID 1846032 の反応式
[Br:1][C:2]1[CH:7]=[CH:6][C:5](F)=[CH:4][C:3]=1[CH:9]([F:11])[F:10].[CH2:12]([S-:14])[CH3:13].[Na+].O>CS(C)=O>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([S:14][CH2:12][CH3:13])=[CH:4][C:3]=1[CH:9]([F:11])[F:10]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 962WaterHCID 4459711Sodium ethanethiolateHCID 463116681-Bromo-2-(difluoromethyl)-4-fluorobenzene

生成物 1

HCID 90217539(4-Bromo-3-(difluoromethyl)phenyl)(ethyl)sulfane収率 28.4%

試薬・触媒・溶媒 1

HCID 679Dimethyl Sulfoxide溶媒

実験手順

1-Bromo-2-(difluoromethyl)-4-fluorobenzene (Preparation 50, 772 mg, 3.43 mmol) and sodium ethanethiolate (352.7 mg, 3.77 mmol) in DMSO (5 mL) was heated at 50° C. for 18 hours. On cooling, water (70 mL) was added to the reaction mixture, the product was extracted with EtOAc (20 mL×3). The combined organic layers were concentrated to give the crude product, which was purified by silica gel column chromatography eluting with heptane to afford the title compound as a colourless oil (260 mg, 28%).

後処理

  1. temperatureOn cooling
  2. extractionthe product was extracted with EtOAc (20 mL×3)
  3. concentrationThe combined organic layers were concentrated
  4. customto give the crude product, which
  5. customwas purified by silica gel column chromatography
  6. washeluting with heptane

出典と根拠

ORDレコード
ord-89e88194f2824ebc84ffce6e64c82f06
出典データセット
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08952008B2

反応ノート

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