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4-Methylbenzyl chloride → 1-Chloro-4-[[(4-methylphenyl)methyl]thio]benzene

HRID 2231791
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반응식

HRID 2231791 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([SH:8])=[CH:4][CH:3]=1.[OH-].[K+].[CH3:11][C:12]1[CH:19]=[CH:18][C:15]([CH2:16]Cl)=[CH:14][CH:13]=1>O.[Cl-].C([N+](CC)(CC)CC)C>[CH3:11][C:12]1[CH:19]=[CH:18][C:15]([CH2:16][S:8][C:5]2[CH:6]=[CH:7][C:2]([Cl:1])=[CH:3][CH:4]=2)=[CH:14][CH:13]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 77224-Methylbenzyl chlorideHCID 7815p-ChlorothiophenolHCID 14797Potassium Hydroxide

생성물 1

HCID 130603691-Chloro-4-[[(4-methylphenyl)methyl]thio]benzene

시약·촉매·용매 2

HCID 5946Tetraethylammonium Chloride촉매HCID 962Water용매2회
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실험 절차

150 g of 4-chlorothiophenol in 200 ml of water, 65 g of potassium hydroxide, 10 g of tetraethylammonium chloride and 140 g of 4-methylbenzyl chloride are initially introduced into a stirred apparatus and are heated under reflux for 4 hours. 300 ml of water are then added, and the mixture is cooled. The solid product is filtered off under suction and washed with water. After the crystals have been dried, 230 g of product of melting point 72° to 73° C. remain.

후처리

  1. temperatureare heated
  2. temperatureunder reflux for 4 hours
  3. temperaturethe mixture is cooled
  4. filtrationThe solid product is filtered off under suction
  5. washwashed with water
  6. customAfter the crystals have been dried

출처 및 근거

ORD 기록
ord-2729507f7eec4b98bcb261f5f21692fd
출처 데이터셋
uspto-grants-1988_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04783562

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