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Water → 4-methylphenyl mesitylenesulfonate

HRID 1031848
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인쇄 미리보기

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HRID 1031848 반응식
[CH:1]1[C:6]([OH:7])=[CH:5][CH:4]=[C:3]([CH3:8])[CH:2]=1.[OH-].[Na+].O.[C:12]1([CH3:24])[CH:17]=[C:16]([CH3:18])[CH:15]=[C:14]([CH3:19])[C:13]=1[S:20](Cl)(=[O:22])=[O:21]>C1(C)C=CC=CC=1>[C:12]1([CH3:24])[CH:17]=[C:16]([CH3:18])[CH:15]=[C:14]([CH3:19])[C:13]=1[S:20]([O:7][C:6]1[CH:5]=[CH:4][C:3]([CH3:8])=[CH:2][CH:1]=1)(=[O:21])=[O:22]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 2879P-CresolHCID 130462-Mesitylenesulfonyl chlorideHCID 14798Sodium Hydroxide

생성물 1

HCID 43428334-methylphenyl mesitylenesulfonate

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

10.8 g of p-cresol is added to a mixture containing 9.17 g of 48% NaOH, 50 ml of water and 50 ml of toluene. To the resulting mixture is added 22.9 g of mesitylenesulfonyl chloride, and reaction is carried out at 60° to 65° C. for 1 hour. After separating the aqueous layer, toluene is removed from the toluene layer by distillation. The resulting desired compound is purified with methanol.

후처리

  1. additionTo the resulting mixture is added
  2. customAfter separating the aqueous layer, toluene
  3. customis removed from the toluene layer by distillation
  4. customThe resulting desired compound is purified with methanol

출처 및 근거

ORD 기록
ord-416cb5f1dac745efa0410d9f45bb1eae
출처 데이터셋
uspto-grants-1990_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04956333

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