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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2052017생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물FosmidomycinHCID 572—
반응물4-Chlorobenzoyl chlorideHCID 8501—
반응물SodiumHCID 5360545—
용매AcetoneHCID 180—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
용매Sodium HydroxideHCID 14798—
생성물3-[N-(p-chlorobenzoyloxy)-N-formylamino] propylphosphonic acidHCID 2033722775.3%

반응 단계

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.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04182758
출처 데이터셋uspto-grants-1980_01
ORD IDord-14da13d93de2418b9ef8e4a476e5df7d
출처 메모uspto-grants-1980_01