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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1472497생성일: 2026년 10월 25일

Acetic Anhydride → rac-Linezolid

https://huagongshe.com/reaction/1472497

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AnhydrideHCID 7918—
반응물TriethylamineHCID 8471—
반응물Tetrafluoro-m-phenylenediamine dihydrochlorideHCID 149026—
반응물3-Fluoro-4-morpholinylphenyl-5-aminomethyl-1,3-oxazolidin-2-oneHCID 22714579—
용매DichloromethaneHCID 6344—
생성물rac-LinezolidHCID 392985%

반응 단계

To a reaction flask were added 6.53 mmol of dihydrochloride of 3-(3-fluoro-4-morpholinylphenyl-5-aminomethyl-1,3-oxazolidin-2-one (5a), 100 ml of dichloromethane and 2.95 ml (21.2 mmol) of triethylamine. Then 0.8 ml (8.45 mmol) of acetic anhydride was added while being stirred in an ice-bath. The mixture was then allowed to react at room temperature for 2 hours before being washed successively with 5% aqueous NaOH solution and saturated aqueous NaCl solution. The organic layer was then dried by anhydrous sodium sulfate and filtered, and subsequently put under reduced pressure for solvent removal. The residue was then subjected to recrystallization using ethyl acetate to give white needle crystals at a yield of 85%, HR-TOF-MS (+Q) m/z: 338.1520 (Calculated [C16H20FN3O4+H]+: 338.1516).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09012631B2
출처 데이터셋uspto-grants-2015_04
ORD IDord-105550dc7a56445f8ca6182f96d8c40a
출처 메모uspto-grants-2015_04