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Phenol → Ethyl 3,3-dimethylpent-4-enoate

HRID 359165
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HRID 359165 반응식
[CH3:1][C:2]([CH3:6])=[CH:3][CH2:4]O.[C:7]([O-:13])([O-])([O:9][CH2:10][CH3:11])[CH3:8].C1(O)C=CC=CC=1>>[CH3:1][C:2]([CH3:6])([CH:3]=[CH2:4])[CH2:8][C:7]([O:9][CH2:10][CH3:11])=[O:13]
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참가 물질

4

반응물 3

HCID 996PhenolHCID 111733-Methyl-2-buten-1-OLHCID 86598186Ethyl ortho-acetate

생성물 1

HCID 82262Ethyl 3,3-dimethylpent-4-enoate수율 78%

실험 절차

A mixture of 43 g (0.5 mole) of 3-methyl-2-buten-1-ol, 97 g (0.6 mole) of ethyl orthoacetate, and 7.0 g (0.075 mole) of phenol was heated at 135°-140° with stirring for 9-10 hours. Ethanol was distilled from the mixture as the reaction proceeded. When the evolution of ethanol had ceased, heating was discontinued and the mixture was allowed to cool to room temperature. The mixture was then dissolved in diethyl ether and the ethereal solution was treated with IN hydrochloric acid to decompose unreacted ethyl orthoacetate. The ethereal solution was then washed successively with a saturated aqueous solution of sodium bicarbonate and with water, then dried over magnesium sulfate. The dried solution was concentrated and distilled under reduced pressure to give 60.8 g (78% yield) of ethyl 3,3-dimethyl-4-pentenoate, b.p. 57°-60°/11 mm.

후처리

  1. temperaturewas heated at 135°-140°
  2. distillationEthanol was distilled from the mixture as the reaction
  3. temperatureheating
  4. dissolutionThe mixture was then dissolved in diethyl ether
  5. additionthe ethereal solution was treated with IN hydrochloric acid
  6. washThe ethereal solution was then washed successively with a saturated aqueous solution of sodium bicarbonate and with water
  7. dry with materialdried over magnesium sulfate
  8. concentrationThe dried solution was concentrated
  9. distillationdistilled under reduced pressure

출처 및 근거

ORD 기록
ord-a1a035ba8ed34526b3eea9222359b618
출처 데이터셋
uspto-grants-1991_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04999451

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