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Water → HCID 23345838, 화합물

HRID 1856093
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HRID 1856093 반응식
[OH:1][N:2]([CH3:21])[C:3](=[O:20])[CH:4]([NH:6][C:7]1[C:12]([N+:13]([O-:15])=[O:14])=[CH:11][C:10]([CH3:16])=[CH:9][C:8]=1[N+:17]([O-:19])=[O:18])[CH3:5].[C:22](N1C=CN(C)C1)(=[O:24])[CH3:23].O>C(Cl)Cl>[C:22]([O:1][N:2]([CH3:21])[C:3](=[O:20])[CH:4]([NH:6][C:7]1[C:12]([N+:13]([O-:15])=[O:14])=[CH:11][C:10]([CH3:16])=[CH:9][C:8]=1[N+:17]([O-:19])=[O:18])[CH3:5])(=[O:24])[CH3:23]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 20532869HCID 20532869, 화합물HCID 21439482HCID 21439482, 화합물

생성물 1

HCID 23345838HCID 23345838, 화합물수율 63.3%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

3 g of N-hydroxy-N-methyl-2-(4-methyl-2,6-dinitrophenylamino)propanamide and 0.82 g of N-acetyl-N'-methylimidazole were added to a stirred suspension in 0.8 g of methylene chloride for 3 hours. The resulting mixture was poured into water. The methylene chloride layer was washed, dried over MgSO4, and evaporated to give a yellow residue which was crystallized from ethanol to yield 1.4 g (41% yield) of product; m.p. 137°-138° C., (d,l) isomer form.

후처리

  1. washThe methylene chloride layer was washed
  2. dry with materialdried over MgSO4
  3. customevaporated
  4. customto give a yellow residue which
  5. customwas crystallized from ethanol

출처 및 근거

ORD 기록
ord-df41294829384c7b9dc9f8642182cdda
출처 데이터셋
uspto-grants-1980_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04218239

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