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Phosphorus oxychloride → Ethyl 2-(2-phenyl-5-isopropyl-4-oxazolyl)acetate

HRID 485004
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HRID 485004 반응식
[C:1]([NH:9][CH:10]([C:17](=[O:21])[CH:18]([CH3:20])[CH3:19])[CH2:11][C:12]([O:14][CH2:15][CH3:16])=[O:13])(=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.P(Cl)(Cl)(Cl)=O>CN(C)C=O>[C:2]1([C:1]2[O:21][C:17]([CH:18]([CH3:19])[CH3:20])=[C:10]([CH2:11][C:12]([O:14][CH2:15][CH3:16])=[O:13])[N:9]=2)[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
참가 물질실험 절차출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24813Phosphorus oxychlorideHCID 13488802Ethyl 3-benzoylamino-3-isobutyrylpropionate

생성물 1

HCID 13488807Ethyl 2-(2-phenyl-5-isopropyl-4-oxazolyl)acetate수율 82%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

6.5 g of ethyl 3-benzoylamino-3-isobutyrylpropionate, 30 ml of dimethylformamide and 4.8 g of phosphorus oxychloride are treated in the same manner as described in Example 1. 5.0 g of ethyl 2-(2-phenyl-5-isopropyl-4-oxazoly)acetate are thereby obtained. Yield: 81.4%.

출처 및 근거

ORD 기록
ord-67ebcf82fdb7482fa0377ebd2f77755b
출처 데이터셋
uspto-grants-1985_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04535089

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