تفاعل #171247
ord-e1342269c6c64ced828ebd7673f082dc
معادلة التفاعل
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1تركيزfollowed by concentration under reduced pressure
- 2workup.DISTILLATIONazeotropic distillation
- 3أخرىAfter completion of the reaction
- 4درجة الحرارةunder ice-cooling
- 5أخرىthe mixture was reacted for 20 min
- 6تركيزThe reaction mixture was concentrated under reduced pressure
- 7workup.ADDITIONWater (150 ml) was added to the concentrate
- 8استخلاصthe mixture was extracted 3 times with ethyl acetate (100 ml)
- 9تركيزThe organic layer was concentrated
- 10أخرىthe obtained oil was purified by silica gel column chromatography
الإجراء التجريبي
Suspending 2′-Deoxycytidine (2.3 g, 10.0 mmol) in dry pyridine, followed by concentration under reduced pressure was repeated 3 times to perform dehydrative azeotropic distillation, the concentrate was suspended again in dry pyridine (60 ml), and trimethylsilyl chloride (6.4 ml, 50 mmol) was added dropwise over 5 min. To the reaction mixture was added 3,5,5-trimethyl-1-hexanoyl chloride (9.5 ml, 50.0 mmol) over 5 min. After completion of the reaction, under ice-cooling, aqueous ammonia (25 ml) was added and the mixture was reacted for 20 min. The reaction mixture was concentrated under reduced pressure. Water (150 ml) was added to the concentrate, and the mixture was extracted 3 times with ethyl acetate (100 ml). The organic layer was concentrated and the obtained oil was purified by silica gel column chromatography to give the title compound (4.7 g).