반응식
[CH:1]1(F)[O:9][C@@H:8]([CH3:10])[C@@H:6]([OH:7])[C@@H:4]([OH:5])[C@@H:2]1O.C(C1C(C(C)(C)C)=NC=CC=1)(C)(C)C.CC[O:28]CC>Cl([O-])(=O)(=O)=O.[Ag+]>[O:9]1[C@H:8]([CH2:10][OH:28])[C@H:6]([OH:7])[C@H:4]([OH:5])[CH:2]=[CH:1]1참가 물질
실험 절차
To 2.00 g (2.47 mmol) of lactal carbonate 8c was added 4.44 g (9.86 mmol) of fucosyl fluoride 9c. The mixture was azeotroped 5 times with benzene and placed under high vacuum for two hours. Under an argon atmosphere 2.77 mL (12.33 mmol) of di-tert-butyl pyridine and 16 mL of dry ether were added. 2.0 g of freshly activated 4 Å molecular sieves were added and the mixture stirred one hour at room temperature. In an argon glove bag, 2.34 g (12.33 mmol) of stannous chloride (SnCl2) and 2.56 g (12.33 mmol) of silver perchlorate (AgClO4) were added. The flask was equipped with a reflux condenser and the reaction brought to reflux for 72 hours. The reaction was quenched with 5 mL of saturated bicarbonate and filtered through a pad of celite. Diluted with 50 mL ethyl acetate and washed 2 times with saturated bicarbonate, 2 times with sat. copper sulfate and 2 times with sat. brine. The organics were dried over MgSO4 and concentrated. Flash chromatography in 20% ethyl acetate/hexanes afforded 2.10 g (51%) of a white foam 10 c:
후처리
- customThe mixture was azeotroped 5 times with benzene
- addition2.0 g of freshly activated 4 Å molecular sieves were added
- customThe flask was equipped with a reflux condenser
- temperatureto reflux for 72 hours
- customThe reaction was quenched with 5 mL of saturated bicarbonate
- filtrationfiltered through a pad of celite
- additionDiluted with 50 mL ethyl acetate
- washwashed 2 times with saturated bicarbonate, 2 times with sat. copper sulfate and 2 times with sat. brine
- dry with materialThe organics were dried over MgSO4
- concentrationconcentrated
출처 및 근거
- ORD 기록
- ord-6f2869f1d0f5443aafd4b6b33e7085c2
- 출처 데이터셋
- uspto-grants-2003_11
- 특허 번호
- US06645935B2
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