戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1419064作成日:2026年10月26日

Acetic Acid → alpha-(4-Benzyloxy-2-methoxyphenyl)-2-neopentylamino-5-chlorobenzyl alcohol

https://huagongshe.com/reaction/1419064

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物PivalaldehydeHCID 12417—
反応物Sodium cyanoborohydrideHCID 5003444—
反応物2-Amino-alpha-(4-benzyloxy-2-methoxyphenyl)-5-chlorobenzyl alcoholHCID 53931958—
溶媒EthanolHCID 702—
生成物alpha-(4-Benzyloxy-2-methoxyphenyl)-2-neopentylamino-5-chlorobenzyl alcoholHCID 54116645—

反応手順

A mixture of 2-amino-α-(4-benzyloxy-2-methoxyphenyl)-5-chlorobenzyl alcohol (9.5 g), pivalaldehyde (3.35 ml), acetic acid (1.85 g) and ethanol (200 ml) was stirred for 30 min. To the mixture was added sodium cyanoborohydride (2.33 g) and the mixture was stirred for 24 h. After the mixture was concentrated in vacuo, the residue was diluted with water (200 ml) and extracted with ethyl acetate (200 ml). The extract was washed with water, dried over magnesium sulfate and concentrated in vacuo. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=5:1) to give α-(4-benzyloxy-2-methoxyphenyl)-2-neopentylamino-5-chlorobenzyl alcohol (10.0 g) as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05885979
出典データセットuspto-grants-1999_03
ORD IDord-c51709c944854e20a4de4b585ef90007
出典メモuspto-grants-1999_03