戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2052005作成日:2026年10月24日

Acetic Anhydride → Fosmidomycin

https://huagongshe.com/ja/reaction/2052005

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AnhydrideHCID 7918—
反応物3-(Hydroxyamino)propylphosphonic acidHCID 342170—
溶媒Formic AcidHCID 284—
生成物FosmidomycinHCID 572—
生成物EthanolamineHCID 700—

反応手順

Formic acid (1.0 ml.) was added dropwise to acetic anhydride (1.2 ml.) at ambient temperature with stirring. The stirring was continued at the same temperature for 30 minutes and then 3-(N-hydroxyamino)propylphosphonic acid (1.51 g.) was added to the mixture. The reaction mixture was stirred at ambient temperature for 1.5 hours and concentrated under reduced pressure to given an oily residue, which was dissolved in ethanol (20 ml.). To the aqueous solution was added ethanolamine (0.61 g.) to precipitate an oil, which was separated by decantation and crystallized with ethanol (20 ml.) to give crystals. The crystals were separated by filtration, washed with ethanol and dried to give crystalline monoethanolamine salt of 3-(N-formyl-N-hydroxyamino)propylphosphonic acid (1.75 g.), a part (1.5 g.) of which was recrystallized from 90% aqueous ethanol to give the purified object compound (1.15 g). M.p. 139°-142° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04182758
出典データセットuspto-grants-1980_01
ORD IDord-8bbfae82b73349da98f7cbfe609f6cb5
出典メモuspto-grants-1980_01