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Ammonium Hydroxide → 5-(4-tert-BUTYLPHENYL)-3-ISOXAZOLECARBOXAMIDE

HRID 1156531
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HRID 1156531 반응식
[C:1]([C:5]1[CH:10]=[CH:9][C:8]([C:11]2[O:15][N:14]=[C:13]([C:16]([O:18]CC)=O)[CH:12]=2)=[CH:7][CH:6]=1)([CH3:4])([CH3:3])[CH3:2].[OH-].[NH4+:22]>O>[C:1]([C:5]1[CH:10]=[CH:9][C:8]([C:11]2[O:15][N:14]=[C:13]([C:16]([NH2:22])=[O:18])[CH:12]=2)=[CH:7][CH:6]=1)([CH3:4])([CH3:3])[CH3:2]
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참가 물질

4

반응물 2

HCID 14923Ammonium HydroxideHCID 20534825Ethyl 5-(4-tert-butylphenyl)-1,2-oxazole-3-carboxylate

생성물 1

HCID 205348295-(4-tert-BUTYLPHENYL)-3-ISOXAZOLECARBOXAMIDE

시약·촉매·용매 1

HCID 962Water용매

실험 절차

Ethyl 5-(4-tert-butylphenyl)-3-isoxazolecarboxylate (25 grams) was mixed with 1 liter of concentrated ammonium hydroxide, and the reaction mixture stirred overnight (about 18 hours) at room temperature. The reaction mixture was then poured into 1 liter of water. The product precipitated and was separated by filtration, yield, 34 grams. The structure of the product was confirmed by NMR.

후처리

  1. customThe product precipitated
  2. customwas separated by filtration
  3. customyield

출처 및 근거

ORD 기록
ord-310fee898a5f45d29ad52811917a6b0e
출처 데이터셋
uspto-grants-1982_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04336264

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