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Nitromethane → 2-amino-1-(2,6-dichlorophenyl)ethan-1-ol

HRID 2053399
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HRID 2053399 반응식
[Cl:1][C:2]1[CH:9]=[CH:8][CH:7]=[C:6]([Cl:10])[C:3]=1[CH:4]=[O:5].[N+:11]([CH3:14])([O-])=O>>[NH2:11][CH2:14][CH:4]([OH:5])[C:3]1[C:2]([Cl:1])=[CH:9][CH:8]=[CH:7][C:6]=1[Cl:10]
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참가 물질

3

반응물 2

HCID 6375NitromethaneHCID 67372,6-Dichlorobenzaldehyde

생성물 1

HCID 186279472-amino-1-(2,6-dichlorophenyl)ethan-1-ol

실험 절차

The method of Schoenenberger, Archiv. der Pharmazie, 1975, 308(9), 717-719 can be employed. 2,6-Dichlorobenzaldehyde can be reacted with nitromethane and base, followed by reduction of the aliphatic nitro group to yield 1-amino-2-hydroxy-2-(2,6-dichlorophenyl) ethane. This substance can be reacted with 4-nitrobenzaldehyde to yield a mixture of cis-(±) and trans-(±)-5-(2,6-dichlorophenyl)-2-(4-nitrophenyl)-1,3-oxazolidines. The nitrophenyl group can be reduced with tin (II) dichloride or iron powder and ammonium chloride to yield the corresponding aniline. This aniline can be reacted with 2,2-dichloroacetyl chloride and triethylamine to yield a mixture of cis-(±) and trans-(±)-2,2-dichloro-N-[4-[5-(2,6-dichlorophenyl)-2-(1,3-oxazolidinyl)]phenyl]acetamides.

출처 및 근거

ORD 기록
ord-a6e36625bf504e89b047837d6ec6429d
출처 데이터셋
uspto-grants-2008_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07326790B2

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