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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1392737Generated: November 3, 2026

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

https://huagongshe.com/reaction/1392737

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-one (J. Org. Chem., 1996, Vol. 61, p. 8687) (89.3 g) was suspended 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 methylene chloride, 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 (41.3 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07342014B2
Source datasetuspto-grants-2008_03
ORD IDord-b7d82b57d1c2434f91d3f3cb95021a01
Source noteuspto-grants-2008_03