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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 855566Generated: October 31, 2026

Cyclopentanol → (4-Bromobutoxy)cyclopentane

https://huagongshe.com/reaction/855566

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 numberUS07262198B2
Source datasetuspto-grants-2007_08
ORD IDord-b21b6695690b4fe69259a0d84059932a
Source noteuspto-grants-2007_08