戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 36560作成日:2026年10月26日

Triethylamine → (S)-3-((tert-Butoxycarbonyl)amino)-5-fluoro-4-oxopentanoic acid

https://huagongshe.com/reaction/36560

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Acetic acid, 2-fluoro-, 1,1'-anhydrideHCID 67886—
反応物N-(tert-butoxycarbonyl)-L-aspartic acidHCID 99718—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒BenzeneHCID 241—
生成物(S)-3-((tert-Butoxycarbonyl)amino)-5-fluoro-4-oxopentanoic acidHCID 10131156—

反応手順

A suspension of Boc-Asp-OH (8.11 mmol) and fluoroacetic anhydride (16.2 mmol) in benzene (30 ml) was treated with triethylamine (16.2 mmol) at room temperature. The catalyst 4-dimethylaminopyridine (0.41 mmol) was added to the solution and the reaction stirred for about 2 h at room temperature. About 100 ml benzene was added to the reaction mixture. The organic solution was washed with 1N HCl (2×50 ml), saturated NaHCO3 (2×50 ml), and saturated NaCl (2×50 ml), followed by drying over anhydrous MgSO4. The solvent was then removed by evaporation under reduced pressure. The resulting oil was applied to a 2.5×80 cm column of silica gel (60-200 mesh). The title compound was eluded with 2% methanol in chloroform.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05416013
出典データセットuspto-grants-1995_05
ORD IDord-1f37921e0a2e4e799336bdb217625c12
出典メモuspto-grants-1995_05