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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1367494Generated: October 29, 2026

Diethyl Ether → tert-Butyl 3-oxocyclopentane-1-carboxylate

https://huagongshe.com/reaction/1367494

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
Reactanttert-ButanolHCID 6386—
Reactant3-Oxocyclopentanecarboxylic acidHCID 227798—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Producttert-Butyl 3-oxocyclopentane-1-carboxylateHCID 1400998696%

Reaction Conditions

Temperature2 °C

Reaction Steps

To a cold (ice bath) solution of 3-oxo-1-cyclopentanecarboxylic acid (1.50 g), tert-butylalcohol (1.05 g) and 4-dimethylaminopyridine (140 mg) in dichloromethane (9 mL) was added a solution of dicyclocarbodiimide in dichloromethane (9 mL). The mixture was stirred 3 hours at ca. 2° C. then diethylether (30 mL) was added and the precipitate was filtered off and discarded. The solution was concentrated in vacuo. The residue was purified by flash chromatography on silica gel with cyclohexane/ethyl acetate (9:1 v/v) as eluant to afford the title compound (1.80 g, 96%) as colorless oil. MS (EI): 111 (M-OtBu.)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893099B2
Source datasetuspto-grants-2011_02
ORD IDord-cd421189375b431ca283a94321e025c6
Source noteuspto-grants-2011_02