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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 703516Generated: October 30, 2026

4-Phenylbutyric Acid → HCID 18642608, compound

https://huagongshe.com/reaction/703516

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Phenylbutyric AcidHCID 4775—
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
ReactantBenzyl octahydrocyclopenta[b]pyrrole-2-carboxylate--hydrogen chloride (1/1)HCID 13216857—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18642608HCID 1864260888%

Reaction Conditions

Temperature0 °C

Reaction Steps

4.92 g (30 mmol) of 4-phenylbutyric acid are dissolved together with 8.4 ml of triethylamine in 200 ml of dry tetrahydrofuran. While cooling in ice, 2.9 ml of ethyl chloroformate are added dropwise. After stirring at 0° C. for 1 hour, 7.4 g of benzyl (2S,3aS,6aS)-octahydrocyclopenta[b]pyrrole-2-carboxylate hydrochloride are added, and the mixture is stirred at room temperature for a further 12 hours. Filtration is followed by concentration, and the residue is taken up in 3% NaHCO3 /ethyl acetate. The organic phase is separated off and washed with 10% strength citric acid, 3% strength NaHCO3 solution and saturated brine, once each, dried with MgSO4 and concentrated. Chromatography on silica gel with ethyl acetate/cyclohexane (1:2) as mobile phase results in 9.05 g of the title compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04983623
Source datasetuspto-grants-1991_01
ORD IDord-b72469dace0946a3868f4b3d0e6e705c
Source noteuspto-grants-1991_01