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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2368758Generated: October 31, 2026

1,5-Dibromopentane → (5-Bromopentyl)cyclohexane

https://huagongshe.com/reaction/2368758

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,5-DibromopentaneHCID 8100—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 178419651HCID 178419651—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product(5-Bromopentyl)cyclohexaneHCID 14952366—

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 1,5-dibromopentane (16 gm, 69.97 mmol) in THF (20 ml) and a solution of (Li2CuCl4 in ether, 14 ml) under nitrogen at 5-10° C. was stirred for 25 minutes and then cyclohexyl magnesium bromide (10 gm, 69.97 mmol) was added dropwise over 30 minutes. The reaction was stirred at 0° C. for another 1 h, then at room temperature for 12 hr. The reaction mixture was cooled to 0° C., saturated with NH4Cl solution (20 ml), diluted with ethyl acetate (100 ml) and the combined organic layer was separated, washed with brine and dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure and the crude product was purified by column chromatography using hexane as an eluent. The pure product was an oily liquid (12.84 gm). 1H NMR (CDCl3): 0.8 (t, 2H, J=10.2 Hz), 1.00-1.38 (m, 9H), 1.52-168 (m, 6H), 1.70-1.80 (m, 2H), 3.38 (t, 2H, J=7.2 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08703798B2
Source datasetuspto-grants-2014_04
ORD IDord-cf3953efd78d4e9696fe43325bc070cb
Source noteuspto-grants-2014_04