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Ammonia → 2-Methyl-2-(4-nitrophenoxy)propanamide

HRID 1725679
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HRID 1725679 반응식
[N+:1]([C:4]1[CH:16]=[CH:15][C:7]([O:8][C:9]([CH3:14])([CH3:13])[C:10](O)=[O:11])=[CH:6][CH:5]=1)([O-:3])=[O:2].ClC(OCC(C)C)=O.C([N:27](CC)CC)C.N>ClCCl.CO>[N+:1]([C:4]1[CH:16]=[CH:15][C:7]([O:8][C:9]([CH3:14])([CH3:13])[C:10]([NH2:27])=[O:11])=[CH:6][CH:5]=1)([O-:3])=[O:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 222AmmoniaHCID 8471TriethylamineHCID 62365Isobutyl chloroformateHCID 1769302-Methyl-2-(4-nitrophenoxy)propanoic acid

생성물 1

HCID 123215222-Methyl-2-(4-nitrophenoxy)propanamide

시약·촉매·용매 2

HCID 887Methanol용매
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HCID 6344
Dichloromethane
용매

실험 절차

A mixture of 2-(4-nitrophenoxy)isobutyric acid (50) (5 g), isobutyl chloroformate (4.36 mL) and triethylamine (8 mL) in dichloromethane (20 mL) was stirred at room temperature for 1 hour. Then 2.0 M ammonia in methanol (20 mL) was added to the solution. The resulting solution was stirred at room temperature for 2 hours and then solvent was removed under reduced pressure. The mixture was purified by recrystallization from EtOAc and hexanes to give 2-(4-nitrophenoxy)-2-methylpropanamide (51).

후처리

  1. stirringThe resulting solution was stirred at room temperature for 2 hours
  2. customsolvent was removed under reduced pressure
  3. customThe mixture was purified by recrystallization from EtOAc and hexanes

출처 및 근거

ORD 기록
ord-6dedb881a9e14c01a5fc25676c66fac6
출처 데이터셋
uspto-grants-2009_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07491732B2

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