反应 #1435775
ord-53a20fc3df5941e8ba2bc65252e79304
反应方程式
反应物
试剂
反应条件
后处理
- 1workup.ADDITIONAfter complete addition
- 2workup.STIRRINGstirring
- 3workup.WAITcontinued at 0° C. for 3 hours
- 4其他at room temperature
- 5其他overnight
- 6其他the solvent was evaporated under reduced pressure
- 7workup.ADDITIONthe residue treated with 100 ml of hydrochloric acid (1 N)
- 8萃取extracted 3 times with 150 ml of ethyl acetate
- 9其他The crude product (4.0 g) was obtained as a dark brown oil which
- 10其他was purified by flash-chromatography on silica gel using a gradient of a 100%
- 11workup.ADDITION0%- to 50%:50%-mixture of heptane and ethyl acetate as the eluent
实验过程
In an inert atmosphere and under exclusion of moisture, at 0° C. a solution of 1.5 g (10 mmol) of 2-methyl-6-nitro-phenol [Ger.Offen. 3536192] in 30 ml of N,N-dimethylformamide was treated portionwise with 0.42 g (18 mmol) of sodium hydride (55% dispersion in mineral oil). After complete addition, stirring was continued for 1 hour at 0° C. Thereafter, 3.85 g (11 mmol) of (S)-2,2-dioxo-2λ6-[1,2,3]oxathiazolidine-3,4-dicarboxylic acid 4-benzyl ester 3-tert-butyl ester was added and stirring continued at 0° C. for 3 hours, then at room temperature overnight. For the working-up, the solvent was evaporated under reduced pressure, the residue treated with 100 ml of hydrochloric acid (1 N), then extracted 3 times with 150 ml of ethyl acetate. The crude product (4.0 g) was obtained as a dark brown oil which was purified by flash-chromatography on silica gel using a gradient of a 100%:0%- to 50%:50%-mixture of heptane and ethyl acetate as the eluent. There were obtained 1.4 g (33%) of the title compound as an yellow oil, [α]589=−1.45° (c=1.0% in MeOH), MS m/e (%): 431.4 (M+H+, 13).