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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1762917Generated: November 2, 2026

Benzyl chloroformate → HCID 53794204, compound

https://huagongshe.com/reaction/1762917

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantAzepane-3-carboxylic acidHCID 13457776—
ProductHCID 53794204HCID 53794204—

Reaction Steps

3-Carboxyhomopiperidine (Source: U.S. Pat. No. 4,409,146) is reacted with benzoxycarbonyl chloride to give 3-(carboxy)-1-homopiperidinecarboxylic acid phenylmethyl ester. This derivative is isolated and reacted with diborane in tetrahydrofuran to give 3-(hydroxymethyl)-1-homopiperidinecarboxylic acid phenylmethyl ester. This derivative is isolated and reacted with pyridinium chlorochromate to give 3-(formyl)-1-homopiperidine carboxylic acid phenylmethyl ester. The epoxide of this derivative is prepared by reacting with trimethyl sulfoxonium iodide and sodium hydride in an aprotic solvent. This epoxide is reacted with sodium phenoxide and the reaction mixture is acidified to give 2-(1-hydroxy-2-phenoxyethyl)-1-homopiperidinecarboxylic acid phenylmethyl ester which is hydrogenated over palladium on carbon to give the free base of the title compound. The free base is then converted to the hydrochloride salt as in Example 38.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04835164
Source datasetuspto-grants-1989_05
ORD IDord-1c308218e6a04207b48466c9ed047548
Source noteuspto-grants-1989_05