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m-Chloroperbenzoic acid → 5-Acetyl-2-(methanesulfinyl)thiophene-3-carbonitrile

HRID 982011
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인쇄 미리보기

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HRID 982011 반응식
ClC1C=CC=C(C(OO)=[O:9])C=1.[CH3:12][S:13][C:14]1[S:15][C:16]([C:21](=[O:23])[CH3:22])=[CH:17][C:18]=1[C:19]#[N:20].C(=O)(O)[O-].[Na+]>C(Cl)Cl.O>[CH3:12][S:13]([C:14]1[S:15][C:16]([C:21](=[O:23])[CH3:22])=[CH:17][C:18]=1[C:19]#[N:20])=[O:9]
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참가 물질

6

반응물 3

HCID 70297m-Chloroperbenzoic acidHCID 516892Sodium BicarbonateHCID 20069010HCID 20069010, 화합물

생성물 1

HCID 200689985-Acetyl-2-(methanesulfinyl)thiophene-3-carbonitrile

시약·촉매·용매 2

HCID 962Water용매HCID 6344Dichloromethane용매

반응 조건

온도
5 °C

실험 절차

5.0 g of 83% m-chloroperbenzoic acid are gradually added while stirring at a temperature of 0°-5° C. in 45 minutes to a solution of 5.0 g of 2-methylthio-3-cyano-5-acetylthiophene in 500 ml of methylene chloride. After stirring for another 30 minutes at 5° C., a saturated solution of sodium bicarbonate in approximately 50 ml of water is added; the reaction mixture is then stirred for 60 minutes. The organic layer is separated, washed with water and dried. After distilling off the solvent, the desired product is obtained in a yield of 4.6 g; melting-point 150° C.

후처리

  1. stirringthe reaction mixture is then stirred for 60 minutes
  2. customThe organic layer is separated
  3. washwashed with water
  4. customdried
  5. distillationAfter distilling off the solvent

출처 및 근거

ORD 기록
ord-dfdb45ae2dc94ab197157b2c2f99f046
출처 데이터셋
uspto-grants-1991_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04994485

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