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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1106334Generated: October 31, 2026

Ethyl chloroformate → HCID 70531549, compound

https://huagongshe.com/reaction/1106334

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 12788506HCID 12788506—
SolventBenzeneHCID 241—
ProductHCID 70531549HCID 70531549—

Reaction Steps

A mixture of 0.45 g of trans-4-(3-methoxyphenoxy)-1-methyl-3-phenylpiperidine, 0.31 g of anhydrous potassium carbonate, 0.22 ml of ethyl chloroformate and 4 ml of anhydrous benzene is stirred for a few minutes at room temperature, then refluxed overnight. Another 0.11 ml of ethyl chloroformate is added, the mixture is refluxed for another 4 hours, then cooled and partitioned between 25 ml of ether and 25 ml of water. The aqueous phase is extracted with another 25 ml of ether, and the combined ether extracts are washed with 2 N hydrochloric acid (2×10 ml), saturated sodium chloride solution (25 ml), dried over anhydrous sodium sulfate and concentrated in vacuo to afford 0.37 g of product as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04312876
Source datasetuspto-grants-1982_01
ORD IDord-66bfd1f6724847b3a37a828b6c64c84b
Source noteuspto-grants-1982_01