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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 475046Generated: October 26, 2026

1,2-Dichloroethane → cyclopentyl (2S)-[(tert-butoxycarbonyl)amino](cyclohexyl)acetate

https://huagongshe.com/reaction/475046

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantCyclopentanolHCID 7298—
Reactant(2S)-2-(((tert-butoxy)carbonyl)amino)-3-cyclohexylpropanoic acidHCID 10588189—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDimethylformamideHCID 6228—
Productcyclopentyl (2S)-[(tert-butoxycarbonyl)amino](cyclohexyl)acetateHCID 57658394235.5%

Reaction Steps

To a solution of (S)-2-tert-butoxycarbonylamino-3-cyclohexyl-propionic acid (5 g, 19.4 mmol) in DMF (50 mL) at 0° C. was added cyclopentanol (8.8 ml, 97.15 mmol), EDC (4.09 g, 21.37 mmol) and finally DMAP (237 mg, 1.94 mmol). The reaction mixture was warmed to RT and stirred for 18 h. The DMF was removed in vacuo to give a clear oil. This was separated between water and EtOAc. The organic phase was dried (MgSO4) and concentrated in vacuo. The crude extract was purified by column chromatography (25% EtOAC in heptane) to yield the desired product as a clear oil (14.87 g, 55%). 1H NMR (300 MHz, d6-DMSO) δ: 7.09 (1H, d), 5.08 (1H, t), 3.76 (1H, t), 1.50-1.85 (10H, br m), 1.39 (9H, s), 1.00-1.25 (9H, br m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637547B2
Source datasetuspto-grants-2014_01
ORD IDord-516d9d60025d492aa40512b535ee8875
Source noteuspto-grants-2014_01