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2-nitrobenzyl-N,N-dimethylsulfonamide → 2-aminobenzyl-N,N-dimethylsulfonamide

HRID 23395
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HRID 23395 반응식
[N+:1]([C:4]1[CH:16]=[CH:15][CH:14]=[CH:13][C:5]=1[CH2:6][S:7]([N:10]([CH3:12])[CH3:11])(=[O:9])=[O:8])([O-])=O>[Pd]>[NH2:1][C:4]1[CH:16]=[CH:15][CH:14]=[CH:13][C:5]=1[CH2:6][S:7]([N:10]([CH3:12])[CH3:11])(=[O:9])=[O:8]
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참가 물질

3

반응물 1

HCID 131787262-nitrobenzyl-N,N-dimethylsulfonamide

생성물 1

HCID 131787272-aminobenzyl-N,N-dimethylsulfonamide수율 96%

시약·촉매·용매 1

HCID 23938Palladium촉매

실험 절차

The 2-nitrobenzyl-N,N-dimethylsulfonamide (0.825 g, 3.377 mmole) of Step 1 was dissolved/suspended in alcohol in a Parr hydrogenation bottle. Palladium on charcoal (90 mg, 10% Pd) was added and the mixture was placed under an atmosphere of hydrogen at 45 psi in a Parr shaker. After shaking overnight, the mixture was filtered through Celite and evaporated to dryness to afford 0.693 g pure 2-aminobenzyl-N,N-dimethylsulfonamide (96% yield).

후처리

  1. filtrationthe mixture was filtered through Celite
  2. customevaporated to dryness

출처 및 근거

ORD 기록
ord-17bcca45b1f247b4b8c6e40e7e9f9671
출처 데이터셋
uspto-grants-2005_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06852726B2

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