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Ammonium Hydroxide → 2-Chloro-5-(4-chlorophenyl)nicotinonitrile

HRID 1995600
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인쇄 미리보기

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HRID 1995600 반응식
[C:1]([C:3]1[C:4](=O)[NH:5][CH:6]=[C:7]([C:9]2[CH:14]=[CH:13][C:12]([Cl:15])=[CH:11][CH:10]=2)[CH:8]=1)#[N:2].C1(P(Cl)([Cl:25])=O)C=CC=CC=1.[NH4+].[OH-]>>[Cl:25][C:4]1[C:3]([C:1]#[N:2])=[CH:8][C:7]([C:9]2[CH:14]=[CH:13][C:12]([Cl:15])=[CH:11][CH:10]=2)=[CH:6][N:5]=1
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참가 물질

4

반응물 3

HCID 14923Ammonium HydroxideHCID 69990Phenylphosphonic dichlorideHCID 27639105-(4-Chlorophenyl)-2-oxo-1,2-dihydropyridine-3-carbonitrile

생성물 1

HCID 27640422-Chloro-5-(4-chlorophenyl)nicotinonitrile

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온도
175 °C

실험 절차

A mixture of 3-cyano-5-(4-chlorophenyl)-2-(1H)-pyridone (2.0 grams) and phenylphosphonic dichloride (3.8 grams) was heated for 4 hours at 175° C. in an oil bath. The mixture was poured into ice water and was made alkaline by stirring with NH4OH. The resulting brownish solid product was used without further purification, yield 2.0 g., m.p. 185°-187° C.

후처리

  1. customThe resulting brownish solid product was used without further purification, yield 2.0 g

출처 및 근거

ORD 기록
ord-b17c418dc7b14ed1b9ec25a8755b141b
출처 데이터셋
uspto-grants-1983_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04405552

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