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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1065033Generated: November 1, 2026

Dichloromethane → HCID 20541129, compound

https://huagongshe.com/reaction/1065033

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantEthyl AcetoacetateHCID 8868—
ReactantPotassium HydroxideHCID 14797—
Reactant1,4-Dichloro-2-butene, (2E)-HCID 642197—
CatalystHCID 178458108HCID 178458108—
ProductHCID 20541129HCID 20541129—

Reaction Conditions

Temperature35 °C

Reaction Steps

Ethyl acetoacetate was reacted with 1,4-dichlorobutene-2 in a manner similar to that described in Example III using a poly(oxypropylene) catalyst. For the reaction, 5.6 g potassium hydroxide and 50 mls. methylene dichloride were combined in the reaction vessel and ethyl acetoacetate (6.5 g), the poly(propylene glycol) catalyst (1.06 g) and 20 mls. methylene dichloride rapidly added with vigorous stirring. 1,4-Dibromobutene-2 (10.7 g) was then added via a solids addition funnel while maintaining the temperature at about 35° C. Seventy-four percent yield 1-carboethoxy-1-methylketo-2-vinylcyclopropane was obtained. The product had a boiling point of 58° C. at 0.85 mm Hg, refractive index (nD25) of 1.4707, and the structure was confirmed by infrared and proton nmr spectroscopy. When the process is repeated reacting 1,4-dichlorobutene-2 with phenylacetonitrile, ethyl phenylacetate and acetoacetanilide, 1-cyano-1-phenyl-2-vinylcyclopropane, 1-carboethoxy-1-phenyl-2-vinylcyclopropane, and 1-carboxanilido-1-methylketo-2-vinylcyclopropane are respectively obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04328169
Source datasetuspto-grants-1982_05
ORD IDord-d50215aadfcb49ceacd303c6e597d345
Source noteuspto-grants-1982_05