تفاعل #162924

معادلة التفاعل

Na2CO3

Na2CO3

tert-butyl ((3S,7S,8R,9S)-7-benzyl-8-((tert-butyldimethylsilyl)oxy)-9-methyl-2-oxo-1,5-dioxonan-3-yl)carbamate

pyridine THF

HF-pyridine

→

tert-butyl-(3S,7S,8R,9S)-7-benzyl-8-hydroxy-9-methyl-2-oxo-1,5-dioxonan-3-ylcarbamate

المردود 90.0%

المذيبات

EtOAc

ظروف التفاعل

المعالجة

1. 1
   أخرىThe crude reaction
2. 2
   workup.ADDITIONwas added
3. 3
   أخرىuntil bubbling
4. 4
   أخرىThe EtOAc layer was separated
5. 5
   استخلاصthe aqueous phase was extracted with EtOAc (2×)
6. 6
   تجفيفThe combined organic layers were dried over Na2SO4
7. 7
   ترشيحfiltered
8. 8
   تركيزconcentrated

الإجراء التجريبي

A solution of tert-butyl ((3S,7S,8R,9S)-7-benzyl-8-((tert-butyldimethylsilyl)oxy)-9-methyl-2-oxo-1,5-dioxonan-3-yl)carbamate (120 mg, 0.24 mmol) in a solution of HF/pyridine/THF (5:3:8 ratio, 1.2 mL) was stirred at room temperature. After 16 h, an additional 0.1 mL HF-pyridine solution was added and the reaction was allowed to stir for 2 h. The crude reaction was diluted with EtOAc (5 mL) and added to sat'd aq Na2CO3 (5 mL) dropwise. Additional sat'd aq Na2CO3 was added until bubbling was no longer observed. The EtOAc layer was separated and the aqueous phase was extracted with EtOAc (2×). The combined organic layers were dried over Na2SO4, filtered, and concentrated to furnish tert-butyl-(3S,7S,8R,9S)-7-benzyl-8-hydroxy-9-methyl-2-oxo-1,5-dioxonan-3-ylcarbamate as a colorless oil (82 mg, 89%): 1H NMR (400 MHz, CDCl3) δ 7.32-7.26 (m, 3H), 7.20 (dd, J=8.2, 6.4 Hz, 2H), 5.15 (d, J=8.5 Hz, 1H), 4.88 (m, 1H), 4.65 (d, J=7.6 Hz, 1H), 3.90 (dd, J=11.7, 7.5 Hz, 1H), 3.57 (d, J=10.3 Hz, 1H), 3.44 (m, 2H), 3.33 (m, 1H), 3.11 (dd, J=13.8, 4.3 Hz, 1H), 2.49 (m, 1H), 1.87 (s, 1H), 1.48 (d, J=6.4 Hz, 3H), 1.43 (d, J=4.3 Hz, 9H); ESIMS m/z 378.4 ([M−H]).

المصدر