1-Isothiocyanato-2-methoxy-4-nitrobenzene → 2-(2-Methoxy-4-nitrophenylimino)-3-cyclooctyl-1,3-thiazolidine

HRID 276340

反応式

HRID 276340 の反応式
[Cl-].[CH:2]1([NH2+:10][CH2:11][CH2:12]Cl)[CH2:9][CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][CH2:3]1.[CH3:14][O:15][C:16]1[CH:21]=[C:20]([N+:22]([O-:24])=[O:23])[CH:19]=[CH:18][C:17]=1[N:25]=[C:26]=[S:27]>>[CH3:14][O:15][C:16]1[CH:21]=[C:20]([N+:22]([O-:24])=[O:23])[CH:19]=[CH:18][C:17]=1[N:25]=[C:26]1[N:10]([CH:2]2[CH2:9][CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][CH2:3]2)[CH2:11][CH2:12][S:27]1

参加物

3

反応物 2

HCID 6108371-Isothiocyanato-2-methoxy-4-nitrobenzeneHCID 18316362N-cyclooctyl-N-(2-chloroethyl)ammonium chloride

生成物 1

HCID 183163722-(2-Methoxy-4-nitrophenylimino)-3-cyclooctyl-1,3-thiazolidine

実験手順

2-Hydroxyethylamine was reacted with cyclooctyl bromide according to Method B2a to give N-cyclooctyl-N-(2-hydroxyethyl)amine. The alcohol was reacted with SOCl2 according to Method B7c to give N-cyclooctyl-N-(2-chloroethyl)ammonium chloride. The chloroethylamine was reacted with 2-methoxy-4-nitrophenyl isothiocyanate to give 2-(2-methoxy-4-nitrophenylimino)-3-cyclooctyl-1,3-thiazolidine.

出典と根拠

ORDレコード
ord-5cf91aec4cee419391cded81bb377bf9
出典データセット
uspto-grants-2002_03
特許番号
US06353006B1

関連ノート

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