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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 26308Generated: October 26, 2026

Water → 3,3-Bis(ethoxycarbonyl)bicyclo[3.2.0]heptane

https://huagongshe.com/reaction/26308

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactanttert-ButanolHCID 6386—
Reactant2,2-DiethylpropanedioateHCID 6951563—
Reactantcis-1,2-Bis(bromomethyl)cyclobutaneHCID 12550420—
ReactantPotassium tert-butoxideHCID 23665647—
Product3,3-Bis(ethoxycarbonyl)bicyclo[3.2.0]heptaneHCID 21325433—

Reaction Steps

In a 250 ml round-bottomed flask equipped with mechanical stirring, reflux condenser, addition funnel and argon inlet was placed 20.2 g of cis-1,2-bis(bromomethyl)cyclobutane, 12.4 ml diethylmalonate, and 72 ml of dry t-butanol. The reaction mixture was refluxed and a solution of 19.9 g of potassium-t-butoxide in 123 ml of t-butanol was added over 6.0 hr. The reaction mixture was refluxed for 15 hr. The reaction mixture was cooled by external application of an ice-water bath and an equal volume of water added. The mixture was extracted with ether. The ether extracts were washed with 3 N hydrochloric acid and 5% aqueous sodium bicarbonate, then dried (MgSO4), filtered and distilled in vacuo to yield 10.3 g of 3,3-bis(ethoxycarbonyl)bicyclo-[3.2.0]heptane as a clear oil, bp 100°-105° C. (vacuum pump).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04149017
Source datasetuspto-grants-1979_04
ORD IDord-fcd33fc4d0d445879007e851f7683803
Source noteuspto-grants-1979_04