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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1579842Generated: November 4, 2026

Pyridine → HCID 21569121, compound

https://huagongshe.com/reaction/1579842

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantEthyl chloroformateHCID 10928—
ReactantHCID 21569107HCID 21569107—
SolventDiethyl EtherHCID 3283—
ProductHCID 21569121HCID 21569121—

Reaction Steps

A solution of α-mercapto-6-methoxy-2-naphthylacetic acid (0.02 moles) in 25 ml. of pyridine is cooled in an ice bath. To this is added dropwise 2.1 mol (0.022 moles) of ethyl chloroformate. The mixture is then stirred for 2 hours, diluted with ether and filtered. The mixture is basified with 10% sodium bicarbonate solution. The alkaline mixture is worked with ether, then acidified with 10% hydrochloric acid, washed with ether, dried and filtered. The solvent is removed and the residue is triturated with hexane to obtain α-ethoxycarbonylthio-6-methoxy-2-naphthylacetic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03931269
Source datasetuspto-grants-1976_01
ORD IDord-0697f90b8eb744779fbe2a74adc098d8
Source noteuspto-grants-1976_01