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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 564688Generated: October 25, 2026

Cyclopentanol → HCID 54144852, compound

https://huagongshe.com/reaction/564688

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopentanolHCID 7298—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantN-[(Phenylmethoxy)carbonyl]-L-isoleucineHCID 2724772—
SolventDichloromethaneHCID 6344—
ProductHCID 54144852HCID 5414485287.4%

Reaction Steps

A solution of N-benzyloxycarbonyl-L-isoleucine (10.0 g, 37.7 mmol) in DCM 150 mL) was treated with N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (7.94 g, 41.5 mmol), cyclopentanol (3.90 g, 45.2 mmol) and N,N-dimethylaminopyridine reaction mixture was washed with 1M hydrochloric acid, saturated sodium bicarbonate, and brine before drying over magnesium sulphate, filtration and removal of solvent under reduced pressure to leave N-benzyloxycarbonyl-L-isoleucine cyclopentyl ester as a colourless oil (10.99 g, 87%). 1H-NMR; δ (CDCl3) 7.44-7.30 (5H, m), 5.37-5.34 (1H, m), 5.22-5.18 (1H, 5.11 (2H, s), 4.33-4.27 (1H, m), 1.90-1.55 (10H, m), 1.51-1.35 (1H, m), 1.28-1.20 (2H, m), 0.93 (3H, d, J 6.9 Hz) and 0.91 (3H, d, J=7.0 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06169075A
Source datasetuspto-grants-2001_01
ORD IDord-2cdf2262962141ddb9beff53b3b02125
Source noteuspto-grants-2001_01