반응 #952553

반응 방정식

acetic anhydride

hydrogen

(R)-[3-(3-fluorophenyl)-2-oxo-5-oxazolidinyl]methyl azide

azide

→

title compound

(S)-N-[[3-(3-fluorophenyl)-2-oxo-5-oxazolidinyl]methyl]acetamide

용매

pyridine

methanol chloroform

ethyl acetate

반응 조건

후처리

1. 1
   기타is consumed
2. 2
   workup.STIRRINGThe reaction mixture is stirred for 1 hr at 20°-25°
3. 3
   여과filtered through Celite
4. 4
   세척washing the pad with ethyl acetate
5. 5
   농축The flitrate is concentrated under reduced pressure
6. 6
   workup.ADDITIONThe addition of ether
7. 7
   기타affords a precipitate
8. 8
   기타After standing in the refrigerator overnight
9. 9
   여과are collected by vacuum filtration
10. 10
    세척washed with cold hexane
11. 11
    기타dried under reducedpressure

실험 절차

A mixture of (R)-[3-(3-fluorophenyl)-2-oxo-5-oxazolidinyl]methyl azide (PREPARATION 16. 8.200 g, 34.71 mol) in ethyl acetate (100 ml) is treated with palladium on carbon (10%, 0.820 g) under nitrogen. The atmosphere is then replaced with hydrogen (balloon) via repeated evacuation and filling. Alter stirring under hydrogen for 17 hr, TLC in methanol/chloroform (5/95) reveals the azide starling material is consumed. The atmosphere is replaced with nitrogen and then pyridine (6 ml) and acetic anhydride (4.1 ml, 43-40 mmol) are added to the reaction mixture. The reaction mixture is stirred for 1 hr at 20°-25° and then filtered through Celite, washing the pad with ethyl acetate. The flitrate is concentrated under reduced pressure and the residue taken-up in dichloromethane. The addition of ether affords a precipitate. After standing in the refrigerator overnight the solids are collected by vacuum filtration, washed with cold hexane, and dried under reducedpressure to give the title compound as a solid. The crude product is purified by chromatography over silica gel, eluting with methanol/chloroform (5/95). The appropriate fractionsare pooled and concentrated to give the title compound, mp 140.0°-140.5°; [α]25 D -6.6° (c 1.0, CHCl3).

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