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Hydrochloric Acid → 3-(Benzyloxy)benzene-1,2-diol

HRID 267785
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인쇄 미리보기

반응식

HRID 267785 반응식
COC1(C)[O:7][C:6]2[CH:8]=[CH:9][CH:10]=[C:11]([O:12][CH2:13][C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=3)[C:5]=2[O:4]1.Cl>CO>[CH2:13]([O:12][C:11]1[CH:10]=[CH:9][CH:8]=[C:6]([OH:7])[C:5]=1[OH:4])[C:14]1[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 21553974HCID 21553974, 화합물

생성물 1

HCID 119774353-(Benzyloxy)benzene-1,2-diol

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A mixture of 2-methoxy-2-methyl-4-benzyloxy-1,3-benzodioxole (13.6 g., 0.05 mole), methanol (210 ml.) and 5N hydrochloric acid (210 ml.) is stirred under reflux in an atmosphere of nitrogen for 10 hours. Most of the methanol is distilled off under vacuum and the product then extracted with ether. The ethereal solution is washed with water, dried over magnesium sulfate followed by calcium sulfate and evaporated to dryness to yield the crude 3-benzyloxy-catechol which can be recrystallized from di-isopropyl ether.

후처리

  1. temperatureunder reflux in an atmosphere of nitrogen for 10 hours
  2. distillationMost of the methanol is distilled off under vacuum
  3. extractionthe product then extracted with ether
  4. washThe ethereal solution is washed with water
  5. dry with materialdried over magnesium sulfate
  6. customevaporated to dryness

출처 및 근거

ORD 기록
ord-cf8fe09b4d854d44912f7654216a4cc3
출처 데이터셋
uspto-grants-1976_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03944560

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