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

HRID 1846021
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HRID 1846021 반응식
[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]
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참가 물질

6

반응물 4

HCID 15413tert-Butyl methyl etherHCID 78037Bromocyclopropane2회HCID 23665647Potassium tert-butoxide2회HCID 265970934-Bromo-3-fluorothiophenol

생성물 1

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

시약·촉매·용매 1

HCID 679
Dimethyl Sulfoxide
용매

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온도
90 °C

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-818f54f89ddf45ccb0f97de2bd06525e
출처 데이터셋
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08952008B2

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