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p-Toluenesulfonic acid → (1,5-Dimethyl-1H-pyrrol-3-yl)(4-methylphenyl)methanone

HRID 1414739
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인쇄 미리보기

반응식

HRID 1414739 반응식
[CH3:1][N:2]1[C:6](C(C2C=CC(C)=CC=2)=O)=[CH:5][CH:4]=[C:3]1[CH3:16].[C:17]1([CH3:27])[CH:22]=[CH:21][C:20](S(O)(=O)=O)=[CH:19][CH:18]=1.[C:28](=[O:31])(O)[O-].[Na+]>>[CH3:1][N:2]1[CH:6]=[C:5]([C:28]([C:20]2[CH:21]=[CH:22][C:17]([CH3:27])=[CH:18][CH:19]=2)=[O:31])[CH:4]=[C:3]1[CH3:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 6101p-Toluenesulfonic acidHCID 516892Sodium BicarbonateHCID 12648628(1,5-Dimethyl-1H-pyrrol-2-yl)(4-methylphenyl)methanone

생성물 1

HCID 12648631(1,5-Dimethyl-1H-pyrrol-3-yl)(4-methylphenyl)methanone

실험 절차

A 1.0g sample of 1,2-dimethyl-5-p-toluoylpyrrole in 10g of dried p-toluenesulfonic acid heated at 105° C for 1 hour. The solution is then poured into sodium bicarbonate solution and extracted into chloroform. The chloroform is evaporated in vacuo and the residue is recrystallized from ethyl acetate to give 1,2-dimethyl-4-p-toluoylpyrrole as a tan solid; m.p. 117°-119° C.

후처리

  1. extractionextracted into chloroform
  2. customThe chloroform is evaporated in vacuo
  3. customthe residue is recrystallized from ethyl acetate

출처 및 근거

ORD 기록
ord-fb857c9ae75747ef8f872f0616f87a7a
출처 데이터셋
uspto-grants-1977_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04002643

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