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4-Isopropylaniline → 2-amino-N-(4-isopropylphenyl)benzamide

HRID 1846307
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반응식

HRID 1846307 반응식
[NH:1]1[C:6]2[CH:7]=[CH:8][CH:9]=[CH:10][C:5]=2[C:4](=[O:11])OC1=O.[CH:13]([C:16]1[CH:22]=[CH:21][C:19]([NH2:20])=[CH:18][CH:17]=1)([CH3:15])[CH3:14]>CN(C=O)C>[NH2:1][C:6]1[CH:7]=[CH:8][CH:9]=[CH:10][C:5]=1[C:4]([NH:20][C:19]1[CH:21]=[CH:22][C:16]([CH:13]([CH3:15])[CH3:14])=[CH:17][CH:18]=1)=[O:11]
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참가 물질

4

반응물 2

HCID 74644-IsopropylanilineHCID 8359Isatoic Anhydride

생성물 1

HCID 28065462-amino-N-(4-isopropylphenyl)benzamide

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

A solution of 1H-benzo[d][1,3]oxazine-2,4-dione (2.0 g, 12.2 mmol) and 4-isopropylaniline (1.92 mL, 13.5 mmol) in anhydrous DMF (10 mL) was stirred at 115° C. for 6 hours under nitrogen. DMF was removed and the residue was mixed with water (100 mL) and dichloromethane (150 mL). The organic phase was separated and washed with brine (50 mL). The solvent was removed and the residue was washed with ether (50 mL) to give 2-amino-N-(4-isopropyl-phenyl)-benzamide as a solid. Yield: 0.80 g (25.8%).

후처리

  1. customDMF was removed
  2. additionthe residue was mixed with water (100 mL) and dichloromethane (150 mL)
  3. customThe organic phase was separated
  4. washwashed with brine (50 mL)
  5. customThe solvent was removed
  6. washthe residue was washed with ether (50 mL)

출처 및 근거

ORD 기록
ord-01fc900d4dd64fcbbf2c0b781848793e
출처 데이터셋
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08952021B2

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