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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2299226Generated: October 26, 2026

Bromocyclopentane → Di-n-butyl cyclopentylmalonate

https://huagongshe.com/reaction/2299226

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromocyclopentaneHCID 8728—
ReactantSodium hydrideHCID 24758—
ReactantPropanedioic acid, dibutyl esterHCID 136925—
SolventTetrahydrofuranHCID 8028—
ProductDi-n-butyl cyclopentylmalonateHCID 1838009923.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

A 0.5-liter three-neck flask equipped with a stirrer was purged with nitrogen gas, and 7.2 g (0.3 mols) of sodium hydride and 250 ml of dewatered tetrahydrofuran were put thereinto in a nitrogen stream atmosphere. With stirring, the mixture was cooled to 0° C., and, while its temperature was kept cooled, 66 ml (0.3 mols) of di-n-butyl malonate was dropwise added thereto over a period of 30 minutes. After the addition, the mixture was heated up to room temperature, and 32 ml of cyclopentyl bromide was dropwise added thereto, and refluxed for 5 hours. After this was cooled to room temperature, 10 g of sodium hydride and 32 ml of cyclopentyl bromide were added thereto, and refluxed further for 8 hours. The resulting reaction mixture was washed with 200 ml of water, and subjected to distillation under reduced pressure to obtain 20 g of di-n-butyl cyclopentylmalonate. The yield was 23.5%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06495639B1
Source datasetuspto-grants-2002_12
ORD IDord-609d343da9614d96b332cf876dadeb09
Source noteuspto-grants-2002_12