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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2067936Generated: October 31, 2026

Trichloroacetyl chloride → HCID 68709804, compound

https://huagongshe.com/reaction/2067936

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrichloroacetyl chlorideHCID 6420—
ReactantHCID 68707181HCID 68707181—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductHCID 68709804HCID 68709804—

Reaction Steps

A solution of 7.49 g 1-(1-Ethoxy-vinyl)-4-Fluorobenzene in 3.6 mL of Pyridine was added at 0° C. to 8.19 g of Trichloroacetyl chloride. The suspension was diluted with 15 ml of dry methylene chloride and stirred at room temperature overnight. The resulting dark brown suspension was concentrated in vaccuo, filtered over a silica gel column with a 9:1 mixture of Heptane and Ethyl acetate as eluant. One obtains after concentration 28 g of a reddish brown oil which was repurified by chromatography on silica gel using a 19:1 mixture of Heptane and Ethyl acetate as eluant. The obtained brown oil (10.15 g) was directly used in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08293916B2
Source datasetuspto-grants-2012_10
ORD IDord-1f944542ec6240d38d4c6de0dc484b5f
Source noteuspto-grants-2012_10