1,1-Bis(propan-2-yl) 3,3-dimethoxycyclobutane-1,1-dicarboxylate → [1-(Hydroxymethyl)-3,3-dimethoxycyclobutyl]methanol

Diisopropyl 3,3-dimethoxy-cyclobutane-1,1-dicarboxylate (6.0 g, 20.8 mmol), prepared as described by P. E. Pigou and C. H. Schiesser, J Org Chem, 53, 3841-3 (1988), was dissolved in 200 mL of anhydrous diethyl ether and the ether solution was cooled to 0° C. with stirring under a nitrogen atmosphere. Lithium aluminum hydride (1.6 g, 42 mmol) was added to the ether solution in portions and the reaction mixture was stirred at 0° C. for 0.5 h. The reaction was then quenched by the addition of 1.6 mL of water, followed by 1.6 mL of 15% aqueous sodium hydroxide solution and 4.8 mL of water. The reaction mixture was filtered, the filter cake washed with diethyl ether and the combine ether filtrates were concentrated under reduced pressure. The residue (3.0 g) was dissolved in 2 mL of methylene chloride and purified on a 1.5×45 cm silica gel column eluted @ 2-3 psi with 200 mL of acetone:hexane (1:2 v/v), followed by 200 mL of acetone:hexane (1:1 v/v) to give 1.51 g (41% yield) of the title compound; MS DCI/NH3M-Z: 194 (M+NH4)+ ; 1H NMR (CDCl3) δ 1.99 (s, 4H), 2.35 (t, 2H-OH), 3.16 (s, 6H), 3.77 (d, 4H).

1. stirringthe reaction mixture was stirred at 0° C. for 0.5 h
2. customThe reaction was then quenched by the addition of 1.6 mL of water
3. filtrationThe reaction mixture was filtered
4. washthe filter cake washed with diethyl ether
5. concentrationthe combine ether filtrates were concentrated under reduced pressure
6. dissolutionThe residue (3.0 g) was dissolved in 2 mL of methylene chloride
7. custompurified on a 1.5×45 cm silica gel column
8. washeluted @ 2-3 psi with 200 mL of acetone:hexane (1:2 v/v)

ORD-Eintrag

ord-498232fddde34261911c12c5c23147f0

Quelldatensatz

uspto-grants-1993_09

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US05246931