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Methanol → Methyl 2-chloro-5-(trifluoromethyl)pyridine-4-carboxylate

HRID 2386799
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HRID 2386799 반응식
[C:1](Cl)(=O)C(Cl)=O.[Cl:7][C:8]1[CH:9]=[C:10]([C:14]([C:17]([F:20])([F:19])[F:18])=[CH:15][N:16]=1)[C:11]([OH:13])=[O:12].CO>C(Cl)Cl.CN(C=O)C>[CH3:1][O:12][C:11](=[O:13])[C:10]1[C:14]([C:17]([F:20])([F:18])[F:19])=[CH:15][N:16]=[C:8]([Cl:7])[CH:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 887MethanolHCID 65578Oxalyl chlorideHCID 112646082-Chloro-5-(trifluoromethyl)isonicotinic acid

생성물 1

HCID 71299630Methyl 2-chloro-5-(trifluoromethyl)pyridine-4-carboxylate

시약·촉매·용매 2

HCID 6228Dimethylformamide촉매HCID 6344Dichloromethane용매

실험 절차

Oxalyl chloride (0.5 ml) was added to a solution of 2-chloro-5-(trifluoromethyl)isonicotinic acid (CAS Reg. No. 505084-58-2, 68 mg) in DCM (5 ml). DMF (1 drop) was added and the resulting mixture was stirred overnight at room temperature. Methanol (5 ml) was added and the mixture was concentrated to dryness. The crude product was used in the next step without further purification.

후처리

  1. concentrationthe mixture was concentrated to dryness
  2. customThe crude product was used in the next step without further purification

출처 및 근거

ORD 기록
ord-392ec75cd9614ab18dd961e4217e665d
출처 데이터셋
uspto-grants-2012_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08268820B2

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