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Dimethylformamide → 6-Chloro-8-nitro-4H-benzo[1,4]oxazin-3-one

HRID 1505193
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HRID 1505193 반응식
[NH2:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[C:4]([N+:9]([O-:11])=[O:10])[C:3]=1[OH:12].CN([CH:16]=[O:17])C.[C:18]([O-])([O-])=O.[K+].[K+]>>[Cl:8][C:6]1[CH:5]=[C:4]([N+:9]([O-:11])=[O:10])[C:3]2[O:12][CH2:18][C:16](=[O:17])[NH:1][C:2]=2[CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 6228DimethylformamideHCID 11430Potassium CarbonateHCID 43482942-Amino-4-chloro-6-nitrophenol

생성물 1

HCID 116515356-Chloro-8-nitro-4H-benzo[1,4]oxazin-3-one수율 19%

실험 절차

To a solution of 2-amino-4-chloro-6-nitrophenol (5 g, 26.5 mmol) in DMF (20 ml) ethylbromoacetate (3 ml, 26.5 mmol) and K2CO3 (4 g, 29.15 mmol) were added and the reaction was stirred at room temperature for 20 hours. The solvent was evaporated and the crude was dissolved in AcOEt (30 ml) and washed with NaOH 5%, water and brine. The organic phase was dried over sodium sulfate and concentrated under vacuum. The purification of the crude residue by crystallization from ether/AcOEt gave 1.13 g of a beige solid. Yield: 19%. 1HNMR (DMSO, 200 MHz) δ 4.79 (2H, s), 7.15 (1H, d, J=2.6 Hz), 7.66 (1H, d, J=2.8 Hz), 11.21 (1H, bs)

후처리

  1. customThe solvent was evaporated
  2. dissolutionthe crude was dissolved in AcOEt (30 ml)
  3. washwashed with NaOH 5%, water and brine
  4. dry with materialThe organic phase was dried over sodium sulfate
  5. concentrationconcentrated under vacuum
  6. customThe purification of the crude residue
  7. customby crystallization from ether/AcOEt

출처 및 근거

ORD 기록
ord-1bd52bbbe8ee4d6c9ea40786b720f98f
출처 데이터셋
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09216975B2

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