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Hydrochloric Acid → 4-(3,3-Dichloro-2-propenyloxy)phenol

HRID 369679
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HRID 369679 반응식
C([O:9][C:10]1[CH:15]=[CH:14][C:13]([O:16][CH2:17][CH:18]=[C:19]([Cl:21])[Cl:20])=[CH:12][CH:11]=1)(=O)C1C=CC=CC=1.[OH-].[K+].Cl>CO>[Cl:20][C:19]([Cl:21])=[CH:18][CH2:17][O:16][C:13]1[CH:14]=[CH:15][C:10]([OH:9])=[CH:11][CH:12]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 14797Potassium HydroxideHCID 185046614-(3,3-Dichloro-2-propenyloxy)phenyl benzoate

생성물 1

HCID 111720144-(3,3-Dichloro-2-propenyloxy)phenol수율 87%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A reaction vessel was charged with 44.1 g of 4-(3,3-dichloro-2-propenyloxy)phenyl benzoate and 400 ml of methanol, to which 33 g of 30% potassium hydroxide solution was slowly added dropwise under ice cooling. After stirring for 1 hour, the reaction mixture was weakly acidified by the addition of 10% hydrochloric acid and extracted twice with 150 ml of diethyl ether under salting out. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate and then concentrated to give a crude product. The crude product was subjected to silica gel chromatography, which afforded 26.0 g of 4-(3,3-dichloro-2-propenyloxy)phenol (yield, 87%).

후처리

  1. additionwas slowly added dropwise under ice cooling
  2. extractionextracted twice with 150 ml of diethyl ether under salting out
  3. washwashed with water
  4. dry with materialdried over anhydrous magnesium sulfate
  5. concentrationconcentrated
  6. customto give a crude product

출처 및 근거

ORD 기록
ord-64dad038c0aa4c7da7da63fc825b6a05
출처 데이터셋
uspto-grants-2000_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06140274

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