反应详情

A solution of the compound of example 73 (8.66 g, 23.02 mmol) in THF (150 mL) was treated drop wise with a solution of lithium hydroxide-mono hydrate (1.97 g, 46.04 mmol) in water (150 mL). The reaction was complete after about 1 h, according to TLC analysis. Most of the solvent was evaporated. The residue was partitioned between water and ether. The organic phase was separated and the alkaline phase was extracted again with ether. It was next acidified with HCl (6M) to pH˜1 followed by several extractions with ethyl acetate. The recombined organic layer was dried over sodium sulfate, filtered, and evaporated to give the product as colorless oil. 1H-NMR(CDCl3, 400 MH: 1.88(m, 4H); 2.40(t, J=6.9 Hz, 2H); 4.97,4.96, 5.05(2dd, J1=11.8 Hz. J2=8.1 Hz, 4H); 7.35(m, 10H). 31P-NMR(CDCl3, 400 MHz): 33.15.

1. customMost of the solvent was evaporated
2. customThe residue was partitioned between water and ether
3. customThe organic phase was separated
4. extractionthe alkaline phase was extracted again with ether
5. extractionfollowed by several extractions with ethyl acetate
6. dry with materialThe recombined organic layer was dried over sodium sulfate
7. filtrationfiltered
8. customevaporated