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Methanesulfonyl chloride → N-(3-cyanomethyl-2-methyl-phenyl)-methanesulfonamide

HRID 618234
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HRID 618234 반응식
[NH2:1][C:2]1[C:3]([CH3:11])=[C:4]([CH2:8][C:9]#[N:10])[CH:5]=[CH:6][CH:7]=1.[CH3:12][S:13](Cl)(=[O:15])=[O:14]>N1C=CC=CC=1>[C:9]([CH2:8][C:4]1[C:3]([CH3:11])=[C:2]([NH:1][S:13]([CH3:12])(=[O:15])=[O:14])[CH:7]=[CH:6][CH:5]=1)#[N:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 31297Methanesulfonyl chlorideHCID 221703202-(3-Amino-2-methylphenyl)acetonitrile

생성물 1

HCID 18789726N-(3-cyanomethyl-2-methyl-phenyl)-methanesulfonamide수율 94.5%

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

(3-Amino-2-methyl-phenyl)-acetonitrile (11.1 g) was dissolved in 80 ml of pyridine. The solution was cooled in an ice bath and 11.3g of methanesulfonyl chloride was added. The reaction mixture was removed from the ice bath and stirred at room temperature for 30 minutes; 10 ml of water was added, and the mixture was stirred for 30 minutes, poured into ethyl acetate (EtOAc), washed with cold hydrochloric acid, washed with water, dried, and evaporated to give 16.1 g of N-(3-cyanomethyl-2-methyl-phenyl)-methanesulfonamide as a light yellow solid. ##STR105##

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후처리

  1. temperatureThe solution was cooled in an ice bath
  2. customThe reaction mixture was removed from the ice bath
  3. addition10 ml of water was added
  4. stirringthe mixture was stirred for 30 minutes
  5. additionpoured into ethyl acetate (EtOAc)
  6. washwashed with cold hydrochloric acid
  7. washwashed with water
  8. customdried
  9. customevaporated

출처 및 근거

ORD 기록
ord-1dbd139f37134ff0961d6aa1f9c32186
출처 데이터셋
uspto-grants-1999_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05952362

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