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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 459511Generated: October 30, 2026

Ethanol → Ethyl (1S,3S,6R)-7-oxabicyclo[4.1.0]heptane-3-carboxylate

https://huagongshe.com/reaction/459511

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 13487220HCID 13487220—
ProductEthyl (1S,3S,6R)-7-oxabicyclo[4.1.0]heptane-3-carboxylateHCID 57416186—

Reaction Steps

(1S,4S,5S)-4-Iodo-6-oxabicyclo[3.2.1]octan-7-on (J. Org. Chem., 1996, Vol. 61, p. 8687) (89.3 g) was dissolved in ethanol (810 ml), a 2N aqueous solution (213 ml) of sodium hydroxide was added, and the mixture was then stirred at room temperature for 3 hours. After the solvent was distilled off under reduced pressure, and water was added to the residue to conduct extraction with dichloromethane, the extract was dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified by column chromatography on silica gel (hexane:ethyl acetate=17:3) to obtain the title compound (41.2 g) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07192968B2
Source datasetuspto-grants-2007_03
ORD IDord-65fee0af4f884e62ac1329cb22e69f90
Source noteuspto-grants-2007_03