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Dimethylformamide dimethyl acetal → Ethyl 5-(4-bromophenyl)isoxazole-4-carboxylate

HRID 2391107
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인쇄 미리보기

반응식

HRID 2391107 반응식
[Br:1][C:2]1[CH:15]=[CH:14][C:5]([C:6]([CH2:8][C:9]([O:11][CH2:12][CH3:13])=[O:10])=[O:7])=[CH:4][CH:3]=1.Cl.NO.CO[CH:21](OC)[N:22](C)C>>[CH2:12]([O:11][C:9]([C:8]1[CH:21]=[N:22][O:7][C:6]=1[C:5]1[CH:4]=[CH:3][C:2]([Br:1])=[CH:15][CH:14]=1)=[O:10])[CH3:13]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 78373Dimethylformamide dimethyl acetalHCID 443297Hydroxyamine hydrochlorideHCID 2757149Ethyl 3-(4-bromophenyl)-3-oxopropanoate

생성물 1

HCID 22220993Ethyl 5-(4-bromophenyl)isoxazole-4-carboxylate

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온도
100 °C

실험 절차

A solution of ethyl (4-bromobenzoyl)acetate (1.19 g, 4.39 mmol) in N,N-dimethylformamide dimethyl acetal (10 mL) was stirred at 100° C. for 1 hour. The mixture was concentrated, and the residue was dissolved in EtOH (10 mL). Hydroxylamine hydrochloride (0.454 g, 6.57 mmol) was added, and the reaction was stirred at 100° C. for 1 hour. After cooling to room temperature, the mixture was partitioned between EtOAc and H2O, and the organic layer was separated, dried over MgSO4, filtered, and concentrated. The crude material was purified by silica gel chromatography to give the title compound.

후처리

  1. concentrationThe mixture was concentrated
  2. dissolutionthe residue was dissolved in EtOH (10 mL)
  3. temperatureAfter cooling to room temperature
  4. customthe mixture was partitioned between EtOAc and H2O
  5. customthe organic layer was separated
  6. dry with materialdried over MgSO4
  7. filtrationfiltered
  8. concentrationconcentrated
  9. customThe crude material was purified by silica gel chromatography

출처 및 근거

ORD 기록
ord-a2118f8352144c2a8a953df5ee426bfe
출처 데이터셋
uspto-grants-2012_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08273780B2

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