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HRID 2052017作成日:2026年10月24日

Hydrochloric Acid → 3-[N-(p-chlorobenzoyloxy)-N-formylamino] propylphosphonic acid

https://huagongshe.com/ja/reaction/2052017

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物FosmidomycinHCID 572—
反応物4-Chlorobenzoyl chlorideHCID 8501—
反応物SodiumHCID 5360545—
溶媒AcetoneHCID 180—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
溶媒Sodium HydroxideHCID 14798—
生成物3-[N-(p-chlorobenzoyloxy)-N-formylamino] propylphosphonic acidHCID 2033722775.3%

反応手順

Monosodium salt of 3-(N-formyl-N-hydroxyamino)propylphosphonic acid (2.05 g.) was dissolved in a mixture of 1 N aqueous sodium hydroxide solution (20 ml.), water (10 ml.) and acetone (10 ml.). To the solution was added dropwise a solution of p-chlorobenzoyl chloride (2.10 g.) in dry acetone (5 ml.) at 0°-5° C. with stirring. After the stirring was continued at the same temperature for 30 minutes, ethyl acetate (40 ml.) was added to the reaction mixture and then the resultant mixture was adjusted to pH 1 with 10% hydrochloric acid. The ethyl acetate layer was separated and then the aqueous layer was extracted again with ethyl acetate (20 ml.). The combined ethyl acetate layer was washed with aqueous sodium chloride solution, dried over magnesium sulfate and concentrated under reduced pressure to give an oily residue, which was crystallized with ethylether (40 ml.) to give crystals. The crystals were separated by filtration, washed twice with ethylether (10 ml.) to give crystalline 3-[N-(p-chlorobenzoyloxy)-N-formylamino] propylphosphonic acid (2.71 g.).

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-14da13d93de2418b9ef8e4a476e5df7d
出典メモuspto-grants-1980_01