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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 56422Generated: October 25, 2026

Ethanol → Ethyl 7-oxabicyclo[4.1.0]heptane-3-carboxylate

https://huagongshe.com/reaction/56422

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium HydroxideHCID 14798—
Reactant4-Iodo-6-oxabicyclo[3.2.1]octan-7-oneHCID 13487217—
ProductEthyl 7-oxabicyclo[4.1.0]heptane-3-carboxylateHCID 1569170552%

Reaction Steps

To a suspension of Racemate-4-iodo-6-oxa-bicyclo[3.2.1]octan-7-one (45.0 g, 180 mmol) in ethanol (400 mL) was added 2 N aqueous sodium hydroxide (110 mL, 220 mmol) at room temperature while being stirred, and the resulting mixture was stirred for 3 hours. The reaction mixture was concentrated in a bath at a temperature of 35° C. under reduced pressure. Water (500 mL) was added to the resultant oily matter, and the resulting mixture was extracted with ethyl acetate (500 mL). The organic layer was washed with water (500 mL), dried over anhydrous sodium sulfate, filtered and followed by concentration under reduced pressure. The resultant oily matter was purified by silica gel column chromatography (ethyl acetate:petroleum ether=1:10˜1:5), to thereby give the tile compound (15.9 g, 52%) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434700B2
Source datasetuspto-grants-2016_09
ORD IDord-d301b167702a4d90aa832036daab9239
Source noteuspto-grants-2016_09