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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1462462Generated: November 3, 2026

Ethyl orthoformate → HCID 22827147, compound

https://huagongshe.com/reaction/1462462

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl orthoformateHCID 31214—
ReactantHCID 22827146HCID 22827146—
ReactantHCID 22827148HCID 22827148—
SolventEthanolHCID 702—
ProductHCID 22827147HCID 22827147—

Reaction Steps

Following the procedure of Example 3, substituting trans-(±)-3,4-difluoro-N-methyl-N-[6-oxo-2-(1-azetidinyl)cyclohexyl]benzeneacetamide for the trans-(±)-3,4-dichloro-N-methyl-N-[6-oxo-2-(1-pyrrolidinyl)cyclohexyl]benzeneacetamide in 50 ml of dry ethanol instead of methanol and 5.0 ml of triethylorthoformate instead of trimethylorthoformate, there is formed as product trans-(±)-3,4-difluoro-N-methyl-N-[6,6-diethoxy-2-(1-azetidinyl)cyclohexyl]benzeneacetamide, which is converted to a hydrochloride salt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04460600
Source datasetuspto-grants-1984_07
ORD IDord-90c93ab025004fe6a95a1575b1591915
Source noteuspto-grants-1984_07