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Phosphorus oxychloride → Ethyl [2-(4-chlorophenyl)-5-pentyl-1,3-oxazol-4-yl]acetate

HRID 485009
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반응식

HRID 485009 반응식
[Cl:1][C:2]1[CH:24]=[CH:23][C:5]([C:6]([NH:8][CH:9]([C:16](=[O:22])[CH2:17][CH2:18][CH2:19][CH2:20][CH3:21])[CH2:10][C:11]([O:13][CH2:14][CH3:15])=[O:12])=O)=[CH:4][CH:3]=1.P(Cl)(Cl)(Cl)=O>CN(C)C=O>[Cl:1][C:2]1[CH:24]=[CH:23][C:5]([C:6]2[O:22][C:16]([CH2:17][CH2:18][CH2:19][CH2:20][CH3:21])=[C:9]([CH2:10][C:11]([O:13][CH2:14][CH3:15])=[O:12])[N:8]=2)=[CH:4][CH:3]=1
참가 물질실험 절차출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24813Phosphorus oxychlorideHCID 13488805Ethyl 3-(4-chlorobenzamido)-4-oxononanoate

생성물 1

HCID 13488812Ethyl [2-(4-chlorophenyl)-5-pentyl-1,3-oxazol-4-yl]acetate수율 84.3%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

2.0 g of ethyl 3-(4-chlorobenzoylamino)-3-caproylpropionate, 10 ml of dimethylformamide and 1.0 g of phosphorus oxychloride are treated in the same manner as described in Example 1. 1.6 g of ethyl 2-[2-(4-chlorophenyl)-5-n-pentyl-4-oxazolyl]acetate are thereby obtained. Yield: 84.2%.

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출처 및 근거

ORD 기록
ord-d7e62a2776db4e668bd4782a54e66eab
출처 데이터셋
uspto-grants-1985_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04535089

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