Ethyl Bromide → (Ethylthio)benzene

HRID 2413327

반응식

HRID 2413327 반응식
[C:1]1([S:7][Si](C)(C)C)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.CN(C)P(=O)(N(C)C)N(C)C.[CH2:23](Br)[CH3:24].C(OCC)(=O)C>O>[C:1]1([S:7][CH2:23][CH3:24])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1

참가 물질

6

반응 조건

온도
40 °C

실험 절차

A mixture of 11.52 g (63 mmoles) of phenylthio(trimethyl)silane, 22 ml of hexamethylphosphoric triamide and 18.8 ml (250 mmoles) of ethyl bromide was heated in a bath at 40° C. for 2 hours after which the conversion was complete. A solid formed in the reaction mixture and heating was continued for 1 hour after which the mixture was poured into a mixture of 150 ml of ethyl acetate and 50 ml of water. The ethyl acetate layer was separated and washed sequentially twice with 50 ml of water, 50 ml of a saturated sodium bicarbonate solution and twice with 25 ml of water. The combined water layers were extracted three times with 25 ml of ethyl acetate and the combined organic phases were washed twice with 25 ml of water, dried and evaporated to dryness. The residue was vacuum distilled to obtain 7.25 g (83% yield) of ethyl phenyl sulfide with a boiling point of 81.5°-84° C./14 mm Hg and a refractive index of nD25 =1.5632.

후처리

  1. customA solid formed in the reaction mixture
  2. temperatureheating
  3. customThe ethyl acetate layer was separated
  4. washwashed sequentially twice with 50 ml of water, 50 ml of a saturated sodium bicarbonate solution and twice with 25 ml of water
  5. extractionThe combined water layers were extracted three times with 25 ml of ethyl acetate
  6. washthe combined organic phases were washed twice with 25 ml of water
  7. customdried
  8. customevaporated to dryness
  9. distillationdistilled

출처 및 근거

ORD 기록
ord-945c78cf8e4447758b028a65bedabe2d
출처 데이터셋
uspto-grants-1985_01
특허 번호
US04496720

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