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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2111010Generated: November 3, 2026

Isopropanol → 1-(2-Chloro-1-cyclopentenyl)ethanol

https://huagongshe.com/reaction/2111010

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
Reactant2-Chlorocyclopent-1-ene-1-carbaldehydeHCID 12389970—
ReactantHCID 178418573HCID 178418573—
SolventTetrahydrofuranHCID 8028—
Product1-(2-Chloro-1-cyclopentenyl)ethanolHCID 1418438941.6%

Reaction Steps

Under an argon atmosphere, 2-chloro-1-cyclopentenecarbaldehyde (630 mg, 4.82 mmol) was dissolved in anhydrous tetrahydrofuran (19 ml), methylmagnesium bromide (1.4M toluene solution, 4.1 ml) was added dropwise at 0° C., and the mixture was stirred at room temperature for 30 minutes. Isopropanol (2 ml) was added at 0° C., and the solvent was evaporated under reduced pressure. 1N Hydrochloric acid was added, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride solution and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel chromatography (hexane:ethyl acetate=10:1-6:1) to give the title compound (294 mg, 2.01 mmol, 41.6%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07517996B2
Source datasetuspto-grants-2009_04
ORD IDord-6b7a704ec95a4182aae2e8c3e4be803a
Source noteuspto-grants-2009_04