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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1039725Generated: October 25, 2026

Sodium Carbonate → Benzyl 2-(difluoromethoxy)acetate

https://huagongshe.com/reaction/1039725

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantSodium SulfateHCID 24436—
ReactantBenzyl 2-hydroxyacetateHCID 561337—
Reactant2,2-Difluoro-2-(fluorosulfonyl)acetic acidHCID 2737516—
SolventAcetonitrileHCID 6342—
ProductBenzyl 2-(difluoromethoxy)acetateHCID 67270747—

Reaction Conditions

Temperature45 °C

Reaction Steps

Benzyl 2-hydroxyacetate (3.2 ml, 22.2 mmol), sodium sulfate (0.63 g, 4.4 mmol), and MeCN (34 ml) were placed in a 100 ml two-necked RBF fitted with a magnetic stirrer, a dropping funnel and a refluxing condenser. 2,2-Difluoro-2-(fluorosulfonyl)acetic acid (9.18 ml, 89 mmol) was then added with stirring at 45° C. After addition, the mixture was further stirred for 1 h at this temperature. The reaction mixture was poured into 10% aqueous sodium carbonate and was extracted with diethyl ether, the combined extracts were washed with 10% aqueous sodium carbonate, water, brine, dried over sodium sulfate, and concentrated. The crude material was purified by column chromatography (4:1 Hexanes/EtOAc) to afford the intermediate benzyl 2-(difluoromethoxy)acetate which was dissolved in EtOAc (34 mL). N-Ethyl-N-isopropylpropan-2-amine (0.561 ml, 3.2 mmol) was added and after degassing with nitrogen, palladium on carbon (0.680 g, 0.64 mmol) was added. The reaction was purged with hydrogen and stirred under 50 PSI of hydrogen for 24 hours. The degassed reaction was filtered through a pad of Celite and concentrate to afford the titled product as the amine salt which was used directly for subsequent reaction steps without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08552181B2
Source datasetuspto-grants-2013_10
ORD IDord-80212c1c70e94680b6640921b565c30e
Source noteuspto-grants-2013_10