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Hydroquinone → 4-(3-Bromopropoxy)phenol

HRID 839667
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HRID 839667 반응식
[C:1]1([CH:8]=[CH:7][C:5]([OH:6])=[CH:4][CH:3]=1)[OH:2].[Br:9][CH2:10][CH2:11][CH2:12]Br.C(=O)([O-])[O-].[K+].[K+]>CC(=O)CC>[Br:9][CH2:10][CH2:11][CH2:12][O:2][C:1]1[CH:8]=[CH:7][C:5]([OH:6])=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 785HydroquinoneHCID 80011,3-DibromopropaneHCID 11430Potassium Carbonate

생성물 1

HCID 124399004-(3-Bromopropoxy)phenol

시약·촉매·용매 1

HCID 6569Methyl Ethyl Ketone용매

실험 절차

A mixture of 88.0 g. (0.80 m.) of hydroquinone, 161.6 g. (0.80 m.) of 1,3-dibromopropane and 55.2 g. (0.40 m.) of potassium carbonate in 2 liters of 2-butanone was heated at reflux for 24 hours. The reaction mixture was filtered and the filtrate concentrated in vacuo. The solid and liquid phases of the residue were separated, and the liquid fraction was chromatographed on silica gel using chloroform-acetonitrile (95:5) as the eluant. There was thus obtained 37.2 g. of 4-(3-bromopropyloxy)phenol as a light brown oil which was used directly in the next reaction.

후처리

  1. additionA mixture of 88.0 g
  2. temperatureat reflux for 24 hours
  3. filtrationThe reaction mixture was filtered
  4. concentrationthe filtrate concentrated in vacuo
  5. customThe solid and liquid phases of the residue were separated
  6. customthe liquid fraction was chromatographed on silica gel
  7. customof 4-(3-bromopropyloxy)phenol as a light brown oil which was used directly in the next reaction

출처 및 근거

ORD 기록
ord-23bd87595a53454f8e2b7128ace45f69
출처 데이터셋
uspto-grants-1978_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04096280

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