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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 58849Generated: October 28, 2026

Water → 5-[(3,3-Difluorocyclobutyl)carbonyl]-2,2-dimethyl-1,3-dioxane-4,6-dione

https://huagongshe.com/reaction/58849

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant2,2-Dimethyl-1,3-dioxane-4,6-dioneHCID 16249—
ReactantBenzyl 3,3-difluorocyclobutane-1-carboxylateHCID 56592986—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product5-[(3,3-Difluorocyclobutyl)carbonyl]-2,2-dimethyl-1,3-dioxane-4,6-dioneHCID 6687814976.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of benzyl 3,3-difluorocyclobutanecarboxylate (28 g, 0.12 mol) and Pd/C (5 g) in methanol (150 mL) was hydrogenated for 2 h at ambient temperature. Pd/C was filtered off and the filtrate was concentrated. The residue was dissolved in dichloromethane (200 mL) and cooled to 0° C. DMAP (30.8 g, 0.250 mol), Meldrum's acid (19.6 g, 0.140 mol) and EDCI (26.9 g, 0.140 mol) were added successively. The reaction mixture was stirred overnight at ambient temperature. Water (200 mL) was added and the resulting mixture was extracted with dichloromethane (300 mL×3). The organic extracts were combined, dried over anhydrous sodium sulfate, and concentrated. The residue was purified by flash column chromatography on silica gel (dichloromethane/methanol=100:1 to 20:1) to afford 5-(3,3-difluorocyclobutanecarbonyl)-2,2-dimethyl-1,3-dioxane-4,6-dione (24 g, 74% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434761B2
Source datasetuspto-grants-2016_09
ORD IDord-68641c0f7dfc44e6b677fedc7a36f419
Source noteuspto-grants-2016_09