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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2119095Generated: November 3, 2026

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

https://huagongshe.com/reaction/2119095

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 numberUS04681953
Source datasetuspto-grants-1987_07
ORD IDord-9795b117afad46dbb1300fca3f67c416
Source noteuspto-grants-1987_07