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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2058071Generated: October 29, 2026

Potassium tert-butoxide → Ethyl 3-ethenyl-1,2,2-trimethylcyclopropane-1-carboxylate

https://huagongshe.com/reaction/2058071

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium tert-butoxideHCID 23665647—
ReactantEthyl 6-bromo-2,3,3-trimethylhex-4-enoateHCID 54437039—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 3-ethenyl-1,2,2-trimethylcyclopropane-1-carboxylateHCID 1327916955%

Reaction Steps

A solution of 526 mg (2 mmoles) of ethyl 6-bromo-2,3,3-trimethyl-4-hexenoate in 2 ml of anhydrous tetrahydrofuran was added dropwise to a suspension of 224 mg (2 mmoles) of potassium t-butoxide in 10 ml of tetrahydrofuran. The mixture was heated under reflux for two hours and then allowed to cool to room temperature. An additional 116 mg (1 mmole) of potassium t-butoxide was added, and the mixture again heated under reflux for two hours. The reaction mixture was poured into ice water, and the aqueous mixture extracted with diethyl ether. The ether extract was dried over magnesium sulfate and distilled to give 200 mg (55% yield) of ethyl 1,3,3-trimethyl-2-vinylcyclopropanecarboxylate, b.p. 92°-95°/1.5 mm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04214097
Source datasetuspto-grants-1980_07
ORD IDord-10e30749164d481c9ea392f51070773b
Source noteuspto-grants-1980_07