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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2200346Generated: October 30, 2026

Diethyl Carbonate → Ethyl 6-oxospiro[2.5]octane-5-carboxylate

https://huagongshe.com/reaction/2200346

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl CarbonateHCID 7766—
ReactantSodium hydrideHCID 24758—
ReactantSpiro[2.5]octan-6-oneHCID 19371017—
SolventDimethylformamideHCID 6228—
ProductEthyl 6-oxospiro[2.5]octane-5-carboxylateHCID 2420956435.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of spiro[2.5]octan-6-one (prepared according to the procedure reported in US2008176926) (0.900 g, 7.25 mmol) in dimethylformamide (10 ml) at 5° C. was added sodium hydride (0.580 g, 60%, 14.50 mmol) under a nitrogen atmosphere over a period of 10 min and the resulting mixture was stirred for an additional 20 min at the same temperature. To this reaction mixture, diethylcarbonate (1.72 g, 14.50 mmol) was added at 5° C. and stirred for 1 h and then allowed to stir at room temperature for 2 h. The progress of the reaction was monitored by TLC. The reaction mixture was cooled to 0° C. and quenched with saturated ammonium chloride (10 ml) and diluted with water (30 ml). The resulting mixture was extracted with diethyl ether (2×20 ml), and the combined organic layer was washed with water (2×20 ml), dried over anhydrous sodium sulphate, filtered, and the solvent was removed under reduced pressure to obtain a crude product which was purified by flash chromatography over silica gel (100-200 mesh) using 1% ethyl acetate in hexane as eluent to yield the title compound (0.510 g, 35.9%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09359367B2
Source datasetuspto-grants-2016_06
ORD IDord-e53574cdf32e49b5b98813a82c4a1d80
Source noteuspto-grants-2016_06