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Thiophenol → [(3-Chloro-2-methylpropyl)sulfanyl]benzene

HRID 462250
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인쇄 미리보기

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HRID 462250 반응식
[C:1]1([SH:7])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.Br[CH2:9][CH:10]([CH3:13])[CH2:11][Cl:12].[OH-].[Na+]>C(O)C>[C:1]1([S:7][CH2:9][CH:10]([CH3:13])[CH2:11][Cl:12])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1
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참가 물질

5

반응물 3

HCID 7969ThiophenolHCID 14798Sodium HydroxideHCID 955661-Bromo-3-chloro-2-methylpropane

생성물 1

HCID 12573586[(3-Chloro-2-methylpropyl)sulfanyl]benzene수율 97.1%

시약·촉매·용매 1

HCID 702Ethanol용매

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온도
40 °C

실험 절차

A mixture of 22 g (0.2 mol) of thiophenol and 37.7 g (0.22 mol) of 3-bromo-1-chloro-2-methylpropane in 200 ml of ethanol is stirred at 40° C and 40 ml (0.2 mol) of 5N sodium hydroxide solution is added dropwise. The mixture is stirred for a further 2 hours at 40° C and evaporated to dryness in vacuo, the residue is extracted with methylene chloride and the extract is washed with water, dried and evaporated in vacuo. 39 g (97%) of a yellow oil are obtained.

후처리

  1. stirringThe mixture is stirred for a further 2 hours at 40° C
  2. customevaporated to dryness in vacuo
  3. extractionthe residue is extracted with methylene chloride
  4. washthe extract is washed with water
  5. customdried
  6. customevaporated in vacuo

출처 및 근거

ORD 기록
ord-c3e0945c54d74585a2e00cf4e7e1d543
출처 데이터셋
uspto-grants-1977_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04065584

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