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Potassium Hydroxide → HCID 53977809, 화합물

HRID 1414143
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HRID 1414143 반응식
[CH:1]1([CH2:4][CH2:5][CH2:6][O:7][C:8]2[CH:13]=[CH:12][C:11]([OH:14])=[CH:10][CH:9]=2)[CH2:3][CH2:2]1.[OH-].[K+].[CH2:17]([CH:19]1[O:21][CH2:20]1)Br>O>[CH:1]1([CH2:4][CH2:5][CH2:6][O:7][C:8]2[CH:13]=[CH:12][C:11]([O:14][CH2:17][CH:19]3[O:21][CH2:20]3)=[CH:10][CH:9]=2)[CH2:3][CH2:2]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 14797Potassium HydroxideHCID 18430EpibromohydrinHCID 54190475HCID 54190475, 화합물

생성물 1

HCID 53977809HCID 53977809, 화합물수율 100%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

A mixture of 9 g of 4-cyclopropylpropoxy-phenol, 150 ml of water, 3 g of KOH and 7.7 g of epibromohydrin is stirred for 15 hours at ambient temperature. The reaction mixture is extracted with ether and the extract is washed with N NaOH and then with water. The ether is evaporated and the excess epibromohydrin is removed by entrainment with xylene (distillation at 15 mm Hg). 1-(4-Cyclopropylpropoxy-phenoxy)-2,3-epoxy-propane is obtained in a yield of 100%.

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후처리

  1. extractionThe reaction mixture is extracted with ether
  2. washthe extract is washed with N NaOH
  3. customThe ether is evaporated
  4. customthe excess epibromohydrin is removed by entrainment with xylene (distillation at 15 mm Hg)

출처 및 근거

ORD 기록
ord-0fb487186dca484abcd2edcfbeed596a
출처 데이터셋
uspto-grants-1981_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04252984

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