2-Methyl-4-nitrophenyl isothiocyanate → 2-(2-Methyl-4-nitrophenylimino)-3-cyclooctyl-1,3-thiazolidine

HRID 276337ノート

反応式

HRID 276337 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][C:15]1[CH:20]=[C:19]([N+:21]([O-:23])=[O:22])[CH:18]=[CH:17][C:16]=1[N:24]=[C:25]=[S:26]>>[CH3:14][C:15]1[CH:20]=[C:19]([N+:21]([O-:23])=[O:22])[CH:18]=[CH:17][C:16]=1[N:24]=[C:25]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:26]1

参加物

3

反応物 2

HCID 1456212-Methyl-4-nitrophenyl isothiocyanateHCID 18316362N-cyclooctyl-N-(2-chloroethyl)ammonium chloride

生成物 1

HCID 183165092-(2-Methyl-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-methyl-4-nitrophenyl isothiocyanate to give 2-(2-methyl-4-nitrophenylimino)-3-cyclooctyl-1,3-thiazolidine.

出典と根拠

ORDレコード
ord-68e1a1fa806f4f51a1a6e949a7f6827d
出典データセット
uspto-grants-2002_03
特許番号
US06353006B1

反応ノート

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