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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 280387Generated: October 29, 2026

Methyl cyanoacetate → HCID 13632645, compound

https://huagongshe.com/reaction/280387

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl cyanoacetateHCID 7747—
ReactantPotassium CarbonateHCID 11430—
Reactant18860-95-2HCID 205858—
SolventTetrahydrofuranHCID 8028—
ProductHCID 13632645HCID 13632645102.3%

Reaction Steps

A mixture of 65.3 g of methyl cyanoacetate, 228 g of freshly pulverized potassium carbonate and 800 ml of anhydrous tetrahydrofuran was heated at reflux under nitrogen for 2 hours. A solution of 150.5 g of 1,4-dibromo-2-methyl-2-butene in 500 ml of anhydrous tetrahydrofuran was added slowly dropwise to the refluxing reaction mixture over a period of two days. The solids were removed from the cooled reaction mixture by filtration through a bed of celite. The filtrate was concentrated in vacuo to leave 111.4 g of yellow oil. Distillation of the oil gave 81.3 g of the desired product as a colorless oil: b.p. 95°-105° C. (0.05 mm Hg) consisting of two isomers in a ratio of 2:1 by GLC.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04588821
Source datasetuspto-grants-1986_05
ORD IDord-ea186d174e804d59ae6240a0c212c3c5
Source noteuspto-grants-1986_05