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HRID 19405作成日:2026年10月25日

Ethyl 2-(diphenylmethyleneamino)acetate → (S)-2-(benzhydrylidene-amino)-4-methyl-hexanoic acid ethyl ester

https://huagongshe.com/reaction/19405

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl 2-(diphenylmethyleneamino)acetateHCID 319508—
反応物(S)-(+)-1-Iodo-2-methylbutaneHCID 5702528—
反応物Potassium tert-butoxideHCID 23665647—
溶媒TetrahydrofuranHCID 8028—
生成物(S)-2-(benzhydrylidene-amino)-4-methyl-hexanoic acid ethyl esterHCID 8663524474%

反応条件

温度0 °C

反応手順

A solution of (benzhydrylidene-amino)-acetic acid ethyl ester (5.48 g, 20.5 mmol) in tetrahydrofuran (40 mL) was treated with potassium t-butoxide (2.83 g, 25.26 mmol) and stirred at 0° C. for 35 min. At this time a solution of (S)-1-iodo-2-methyl-butane (5.00 g, 25.25 mmol) in tetrahydrofuran (20 mL) was added via syringe and the resulting solution stirred at 0° C. for 10 min and then room temperature overnight. The reaction mixture was concentrated in vacuo and the residue partitioned between diethyl ether and dilute aqueous hydrochloric acid. The layers were separated, and the organic layer was washed with brine and concentrated in vacuo. The residue was purified by ISCO flash chromatography (RediSep silica 120 g, 0% to 10% ethyl acetate/hexanes) which afforded (S)-2-(benzhydrylidene-amino)-4-methyl-hexanoic acid ethyl ester (5.09 g, 74%) as an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07741327B2
出典データセットuspto-grants-2010_06
ORD IDord-e2b1e4a3f0e64d58bf4a398c4d0d1a9d
出典メモuspto-grants-2010_06