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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2187326Generated: October 30, 2026

Bromide ion → 5-(Cyclopent-1-enyl)-2-methylpentan-2-ol

https://huagongshe.com/reaction/2187326

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromide ionHCID 259—
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl EtherHCID 3283—
Reactant5-(1-Cyclopentenyl)pentan-2-oneHCID 13528009—
Product5-(Cyclopent-1-enyl)-2-methylpentan-2-olHCID 1843387311%

Reaction Steps

5-(Cyclopent-1-enyl)-2-pentanone (5.95 g; 39 mmol) in ethyl ether (6 ml) was added dropwise to a 3M solution of methylnagnesium bromide in the same solvent (17 ml; 51 mmol) during 15 minutes. After 2 hours at reflux, the mixture was cooled down to room temperature, poured into ice (20 g), acidified with 5N HCl (20 ml) and extracted with MTBE (60 ml). The aqueous phase was separated and extracted again with MTBE (2×100 ml). The combined organic phases were washed with saturated NaHCO3 (80 ml), H2O (80 ml), brine (80 ml), dried over MgSO4 and concentrated in vacuo. Bulb-to-bulb distillation (80° C./0.06 torr) yielded quantitatively 5.84 g of 5-(cyclopent-1-enyl)-2-methylpentan-2-ol containing 11% of 5-cyclopentylidene-2-methylpentan-2-ol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06410000B1
Source datasetuspto-grants-2002_06
ORD IDord-13540fe1e8c841bc8238ffba1ff52f14
Source noteuspto-grants-2002_06