反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
5-Aza-spiro[2.4]heptane-5,6-dicarboxylic acid 5-benzyl ester (2.217 g, 7.66 mmol) was dissolved in MeOH (30 mL) and LiOH (1 M in H2O, 15 mL, 15 mmol) was added. After stirring for 15 hours at room temperature, the reaction mixture was poured into 10% HCl and the aqueous phase was extracted 3× with DCM. The combined organics were dried over MgSO4, filtered and concentrated. The residue was treated with MeCN (40 mL), Et3N (1.2 mL, 8.4 mmol) and 2-Bromo-1-(6-bromo-naphthalen-2-yl)-ethanone and the mixture was stirred at room temperature for 20 hours before being filtered over CELITE and concentrated. The resulting oil was dissolved in the minimum amount of DCM and EtOAc (30 mL) was added causing the product to precipitate. The mixture was cooled to 0° C. then the solid was filtered off and rinsed with EtOAc giving clean product (4.00 g, 100%).
WORKUP
后处理
- extractionthe aqueous phase was extracted 3× with DCM
- dry with materialThe combined organics were dried over MgSO4
- filtrationfiltered
- concentrationconcentrated
- stirringthe mixture was stirred at room temperature for 20 hours
- filtrationbefore being filtered over CELITE
- concentrationconcentrated
- dissolutionThe resulting oil was dissolved in the minimum amount of DCM and EtOAc (30 mL)
- additionwas added
- customto precipitate
- temperatureThe mixture was cooled to 0° C.
- filtrationthe solid was filtered off
- washrinsed with EtOAc giving clean product (4.00 g, 100%)