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tert-Butyl methyl ether → (4-Bromo-3-fluorophenyl)(cyclopropyl)sulfane

HRID 1846021
ノート
印刷プレビュー

反応式

HRID 1846021 の反応式
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([SH:8])=[CH:4][C:3]=1[F:9].[CH3:10][C:11]([CH3:14])([O-])C.[K+].BrC1CC1.COC(C)(C)C>CS(C)=O>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([S:8][CH:14]2[CH2:11][CH2:10]2)=[CH:4][C:3]=1[F:9]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 15413tert-Butyl methyl etherHCID 78037Bromocyclopropane2 回HCID 23665647Potassium tert-butoxide2 回HCID 265970934-Bromo-3-fluorothiophenol

生成物 1

HCID 90217816(4-Bromo-3-fluorophenyl)(cyclopropyl)sulfane収率 27.3%

試薬・触媒・溶媒 1

HCID 679
Dimethyl Sulfoxide
溶媒

反応条件

温度
90 °C

実験手順

A stirred mixture of 4-bromo-3-fluorobenzenethiol (Preparation 26, 400 mg, 1.93 mmol), potassium tert-butoxide (238 mg, 2.12 mmol) and bromocyclopropane (701 mg, 5.80 mmol) in DMSO (10 mL) was heated at 90° C. for 16 hours. Additional potassium tert-butoxide (43 mg, 0.386 mmol) and bromocyclopropane (467 mg, 3.86 mmol) were added and heating continued at 90° C. for 30 hours. The mixture was cooled to room temperature and poured into 2-methoxy-2-methylpropane (30 mL). The mixture was washed with water (2×30 mL), dried over Na2SO4, concentrated in vacuo and purified by silica gel column chromatography eluting with heptanes to give the title compound as a colourless oil 27% yield, 130 mg.

後処理

  1. temperatureheating
  2. temperatureThe mixture was cooled to room temperature
  3. washThe mixture was washed with water (2×30 mL)
  4. dry with materialdried over Na2SO4
  5. concentrationconcentrated in vacuo
  6. custompurified by silica gel column chromatography
  7. washeluting with heptanes

出典と根拠

ORDレコード
ord-818f54f89ddf45ccb0f97de2bd06525e
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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