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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 461753Generated: October 26, 2026

Dichloroacetyl chloride → Cyclobutanone, 4-chloro-2,2,3,3-tetramethyl-

https://huagongshe.com/reaction/461753

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloroacetyl chlorideHCID 6593—
Reactant2,3-Dimethyl-2-buteneHCID 11250—
CatalystZincHCID 23994—
SolventIsobutyl ketoneHCID 7958—
ProductCyclobutanone, 4-chloro-2,2,3,3-tetramethyl-HCID 11105656—

Reaction Steps

This process is described in U.S. Pat. No. 4,028,418 Gradual addition of dichloroacetyl chloride to a stirred solution of 2,3-dimethyl-2-butene in diisobutyl ketone containing suspended zinc particles resulted in a yield of 2-chloro-3,3,4,4- tetramethylcyclobutanone of 75%, calculated on starting dichloroacetyl chloride of 3.9, a molar ratio of dichloroacetyl chloride to 2,3-dimethyl-2-butene of 1.3, a temperature of 43° C, zinc in the form of turnings having a largest dimension of 0.841 mm and a starting concentration of 2,3-dimethyl-2-butene of 2.4 mol per liter of diisobutyl ketone. Modifying this experiment by reducing the molar ratio of zinc to dichloroacetyl chloride to 1.1 resulted in a decrease in yield to 51%, the theoretical yield still being 77.4% cf. Example VIII of U.S. Pat. No. 4,028,418.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04064174
Source datasetuspto-grants-1977_12
ORD IDord-35a7febe94054baca872a07bc17841a0
Source noteuspto-grants-1977_12