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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 435445Generated: October 29, 2026

Pyridine → HCID 86738992, compound

https://huagongshe.com/reaction/435445

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 86738993HCID 86738993—
SolventHydrochloric AcidHCID 313—
ProductHCID 86738992HCID 86738992—

Reaction Steps

A mixture of 12.2 g of the product of Step A, 33.5 ml of pyridine and 16.8 ml of acetic acid anhydride was stirred at room temperature for 4 hours and then 40 g of ice were added thereto. The mixture was stirred for 30 minutes and was then poured in a mixture of 60 g of ice-water and 39 ml of concentrated hydrochloric acid. The mixture was stirred for 10 minutes and was extracted with methylene chloride. The organic phase was washed and dried and evaporated to dryness at 50° C. under reduced pressure to obtain 11.8 g of methyl (1R,trans) 2,2-dimethyl-3-(4',4',4'-trichloro-3'-acetoxy-buta-1-enyl)-cyclopropane-1-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04401673
Source datasetuspto-grants-1983_08
ORD IDord-5e23789057fc40a8b30b7bda28c621cf
Source noteuspto-grants-1983_08