戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 276692作成日:2026年10月25日

2-Methyl-4-nitrophenyl isocyanate → (4S)-2-(2-methyl4-nitrophenylimino)-3,4-diisobutyl-1,3-oxazolidine

https://huagongshe.com/reaction/276692

反応式

関与物質

役割名称HCID仕込み量
反応物2-Methyl-4-nitrophenyl isocyanateHCID 4296456—
反応物HCID 22951243HCID 22951243—
生成物(4S)-2-(2-methyl4-nitrophenylimino)-3,4-diisobutyl-1,3-oxazolidineHCID 57001746—

反応手順

(L)-Leucine methyl ester was reduced to (1S)-1-(hydroxymethyl)-3-methylbutylamine according to Method B1b, Step 2. The 2-hydroxyethylamine was reacted with isobutyraldehyde according to Method B4c, Step 1 to afford (4S)-2-isopropyl-4-isobutyl-1,3-oxazolidine. The oxazolidine was reduced according to Method B4c, Step 2 to give (1S)-1-(hydroxymethyl)-N-isobutyl-3-methylbutylamine. The substituted 2-hydroxyethylamine was reacted with SOCl2 according to Method B7b to give (1S)-1-(chloromethyl)-N-isobutyl-3-methylbutylamine. The chloroethylamine was reacted with 2-methyl-4-nitrophenyl isocyanate according to Method C4a to afford (4S)-2-(2-methyl-4-nitrophenylimino)-3,4-diisobutyl-1,3-oxazolidine.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06353006B1
出典データセットuspto-grants-2002_03
ORD IDord-ce7fa2cca60245afbdb2e6f302e9378a
出典メモuspto-grants-2002_03