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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 271225Generated: November 1, 2026

Cyclopentanol → (4-Bromobutoxy)cyclopentane

https://huagongshe.com/reaction/271225

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopentanolHCID 7298—
Reactant1,4-DibromobutaneHCID 8056—
ReactantSodium hydrideHCID 24758—
SolventTolueneHCID 1140—
Product(4-Bromobutoxy)cyclopentaneHCID 21935507—

Reaction Conditions

Temperature0 °C

Reaction Steps

NaH (560 mg, 13.93 mmol, 60% disp. in mineral oil) was washed with hexanes (3×20 mL) in a pressure tube and toluene (6 mL,) was added. The solution was cooled to 0° C. and cyclopentanol (1 g, 11.61 mmol) in toluene (6 mL) was added over 20 min. After stirring at 0° C. for 30 min., 1,4-dibromobutane (1.39 mL, 11.61 mmol) and KI (250 mg) were added. The solution was heated to 100° C. for 14 hours. Upon cooling, the reaction was quenched with NaCl (sat. aq.) and the product extracted with EtOAc. The organic layer was dried over MgSO4, filtered, and concentrated. Purification of the residue via flash column chromatography afforded (4-bromobutoxy)cyclopentane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07452889B2
Source datasetuspto-grants-2008_11
ORD IDord-57207737ad7f4ef8b1d385da84fca41a
Source noteuspto-grants-2008_11