tert-Butanol → 2,3:5,6-Di-O-isopropylidene-D-mannono-1,4-lactone

In a 1000 mL round bottom flask, Dess-Martin periodinane (110 g, 261.62 mmol, Spectrochem, India) was added to a solution of (3aS,6R,6aS)-6-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-ol (45 g, 174 mmol) in anhydrous DCM (900 mL) at rt. The resulting mixture was stirred for 15 minutes and treated with t-BuOH (14.16 g, 191.4 mmol, Rankem, India) at rt. The resulting reaction mixture was stirred at rt for 3 days under an argon atmosphere. Upon completion of the reaction (TLC, 30% EtOAc-hexanes, Rf, 0.55), the reaction mixture was quenched with aqueous Na2S2O3 (1000 mL) and extracted with DCM (4×250 mL). The combined organic extracts were washed with saturated NaHCO3 (500 mL), brine (200 mL), and then dried over anhydrous Na2SO4. The solution was concentrated under reduced pressure, and the residue obtained was washed with n-pentane to give (3aS,6R,6aS)-6-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyldihydrofuro[3,4-d][1,3]dioxol-4(3aH)-one as a colorless solid (35 g, 78%): 1H NMR (400 MHz, CDCl3) δ 4.87 (dd, J=3.2, 5.2 Hz, 1H), 4.83 (d, J=5.2 Hz, 1H), 4.43-4.31 (m, 1H), 4.38-4.37 (m, 1H), 4.13 (dd, J=5.7, 9.2 Hz, 1H), 4.06 (dd, J=5.6, 9.2 Hz, 1H), 1.48 (s, 3H), 1.46 (s, 3H), 1.42 (s, 3H), 1.39 (s, 3H).

1. customThe resulting reaction mixture
2. stirringwas stirred at rt for 3 days under an argon atmosphere
3. customthe reaction mixture was quenched with aqueous Na2S2O3 (1000 mL)
4. extractionextracted with DCM (4×250 mL)
5. washThe combined organic extracts were washed with saturated NaHCO3 (500 mL), brine (200 mL)
6. dry with materialdried over anhydrous Na2SO4
7. concentrationThe solution was concentrated under reduced pressure
8. customthe residue obtained
9. washwas washed with n-pentane

ORD record

ord-b622315313894b5d91812ed7913c8f00

Source dataset

uspto-grants-2016_05

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US09328134B2