Benzenesulfonyl chloride → N-(2-Amino-2-methylpropyl)benzenesulfonamide

HRID 1731766노트

반응식

HRID 1731766 반응식
[NH2:1][CH2:2][C:3]([NH2:6])([CH3:5])[CH3:4].[C:7]1([S:13](Cl)(=[O:15])=[O:14])[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1>C(Cl)(Cl)Cl.N1C=CC=CC=1>[CH3:4][C:3]([NH2:6])([CH3:5])[CH2:2][NH:1][S:13]([C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)(=[O:15])=[O:14]

참가 물질

5

반응물 2

HCID 7369Benzenesulfonyl chlorideHCID 131282-Methylpropylenediamine

생성물 1

HCID 23046101N-(2-Amino-2-methylpropyl)benzenesulfonamide수율 79.1%

시약·촉매·용매 2

HCID 1049Pyridine용매HCID 6212Chloroform용매

반응 조건

온도
0 °C

실험 절차

To a mixture of 14.97 g (0.196 mol) of 1,2-diamino-2-methylpropane in 300 ml of chloroform and 80 ml pyridine at 0° C. was added 10 g (0.057 mol) of benzenesulfonyl chloride at 0° C. The reaction mixture was stirred at 0° C. for 30 minutes and allowed to reach room temperature. The mixture was evaporated to dryness in vacuo and the residue was partitioned between water and chloroform. Evaporation of the chloroform gave 10.3 g (79%) of semisolid. The product was identified by NMR and IR spectroscopy and elemental analysis.

후처리

  1. customto reach room temperature
  2. customThe mixture was evaporated to dryness in vacuo
  3. customthe residue was partitioned between water and chloroform
  4. customEvaporation of the chloroform

출처 및 근거

ORD 기록
ord-4cb733a8e3f544c7a84d1439309aa2fd
출처 데이터셋
uspto-grants-1986_11
특허 번호
US04623652

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