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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 583566생성일: 2026년 10월 26일

Sodium Azide → (5R)-5-(Azidomethyl)-3-(3-fluorophenyl)-2-oxazolidinone

https://huagongshe.com/reaction/583566

반응식

참여 물질

역할이름HCID투입량
반응물Sodium AzideHCID 33557—
반응물(R)-[3-(3-fluorophenyl)-2-oxo-5-oxazolidinyl]methyl 4-methylbenzenesulfonateHCID 54408340—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물(5R)-5-(Azidomethyl)-3-(3-fluorophenyl)-2-oxazolidinoneHCID 11550435—

반응 단계

A mixture of (R)-[3-(3-fluorophenyl)-2-oxo-5-oxazolidinyl]methyl 4-methylbenzenesulfonate (PREPARATION 15, 2.340 g, 6.40 mmol) in dry DMF (60 ml) is treated with solid sodium azide (3.331 g, 51.23 mmmol) at 20-25°. The resultant slurry is warmed to 65° for 4.5 hr and then cooled to 20-25° and left overnight. The reaction mixture is then diluted with ethyl acetate and water, transferred to a separatory funnel, and extracted with ethyl acetate. The combined ethyl acetate extracts are washed thoroughly with water, and then dried (sodium sulfate), filtered and concentrated under reduced pressure to give the title compound, mp 81-82°; [α]25D -136.5° (c 0.9, CHCl3); IR (mineral oil mull): 2115, 1736, 1614, 1591, 1586, 1497, 1422, 1233, 1199, 1081, 1049 cm-1 ; NMR (CDCl3, 300 MHz) δ 7.45, 7.34, 7.23, 6.86, 4.81, 4.09, 3.86, 3.72 and 3.60; MS (m/z) 236 (59.0, M+), 179, 136, 122, 109, 95, 75; HRMS (m/z) 236.0708 (calc'd for C10H9FN4O2 : 236.0709).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05929248
출처 데이터셋uspto-grants-1999_07
ORD IDord-649d99a9f1ee4265b0761a9edfcd6e90
출처 메모uspto-grants-1999_07