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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1696187Generated: November 1, 2026

Oxalyl chloride → HCID 54490493, compound

https://huagongshe.com/reaction/1696187

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 86628631HCID 86628631—
CatalystPyridineHCID 1049—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 54490493HCID 54490493—

Reaction Steps

To a mixture of the compound 2a and 2b obtained in the above step (1) (27.6 g) in methylene chloride (200 mL) were gradually added dropwise oxalyl chloride (31.6 mL) and a few drops of pyridine, and the mixture was refluxed under heating for 4 hours. The reaction mixture was gradually poured in water, and the mixture was extracted with methylene chloride. The organic layer was dried over magnesium sulfate and filtered. The filtrate was concentrated in vacuo to give methyl 3-chloro-2-cyano-4,4,4-trifluoro-2-butenoate as a crude product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163759B2
Source datasetuspto-grants-2012_04
ORD IDord-863e1058b2664211985356a0d74951fd
Source noteuspto-grants-2012_04