反应 #1435771

反应方程式

(S)-2-tert-butoxycarbonylamino-3-hydroxy-propionic acid benzyl ester

2-chloro-6-nitrophenol

triphenylphosphine

diethyl azodicarboxylate

→

title compound

收率 50.9%

(S)-2-tert-Butoxycarbonylamino-3-(2-chloro-6-nitro-phenoxy)-propionic acid benzyl ester

收率 50.9%

溶剂

tetrahydrofurane

反应条件

后处理

1. 1
   workup.WAITthe reaction mixture was left
2. 2
   温度to warm to room temperature
3. 3
   workup.STIRRINGAfter stirring for 18 hours
4. 4
   其他was evaporated under reduced pressure
5. 5
   其他the residue triturated in ether at 0° C
6. 6
   过滤The precipitated triphenylphosphinoxide was filtered
7. 7
   洗涤washed with ether
8. 8
   其他The combined filtrates were evaporated
9. 9
   其他to yield 12.8 g of the crude product as a brown-yellow oil
10. 10
    其他The crude product was purified by chromatography on silica gel

实验过程

Under an inert atmosphere, a solution of 6.5 g (25 mmol) of triphenylphosphine in 20 ml of tetrahydrofurane was treated with at 0° C. with 3.9 ml (25 mmol) of diethyl azodicarboxylate. Thereupon, 3.0 g (17 mmol) of 2-chloro-6-nitrophenol were added and the reaction mixture was stirred at 0° C. for 15 minutes. Finally, 4.93 g (17 mmol) of (S)-2-tert-butoxycarbonylamino-3-hydroxy-propionic acid benzyl ester were added and the reaction mixture was left to warm to room temperature. After stirring for 18 hours, for the working-up the solvent was evaporated under reduced pressure and the residue triturated in ether at 0° C. The precipitated triphenylphosphinoxide was filtered and washed with ether. The combined filtrates were evaporated to yield 12.8 g of the crude product as a brown-yellow oil. The crude product was purified by chromatography on silica gel using heptane and ethyl acetate as the eluent. There were obtained 3.9 g (50%) of the title compound as a yellow oil, [α]589=−5.96° (c=1.0% in MeOH), MS m/e (%): 468.1 (M+NH4+, 100).

来源