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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 719123Generated: November 1, 2026

Water → 1-(4-Chloro-phenyl)-3-cyclopentyl-propan-1-one

https://huagongshe.com/reaction/719123

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantChlorobenzeneHCID 7964—
Reactant3-Cyclopentylpropionyl chlorideHCID 66039—
ReactantAluminum(III) ChlorideHCID 6451240—
Solvent1,2-DichloroethaneHCID 11—
Product1-(4-Chloro-phenyl)-3-cyclopentyl-propan-1-oneHCID 2189690025.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

Aluminum chloride (4.979 g, 37.34 mmol) was added in small portions to a solution of 3-cyclopentylpropionyl chloride (3 g, 18.67 mmol) in 1,2-dichloroethane (100 mL) cooled to 0° C. After 15 min., chlorobenzene (6.304 g, 56.01 mmol) was added. The reaction mixture was stirred at 0° C. for 1 h and at room temperature for 48 h. It was then poured into a mixture of ice and water. The product was extracted with ethyl acetate. The organic layers were washed with saturated solution of sodium bicarbonate (1×30 mL), brine (1×20 mL) and dried over anhydrous magnesium sulfate. The solids were then filtered off, and the filtrate was concentrated in vacuo. Purification of the crude residue by flash chromatography (Biotage system, KP-Sil™ 32–63 μm, 60 Å silica gel) eluting with hexanes yielded 1-(4-chloro-phenyl)-3-cyclopentyl-propan-1-one (1.12 g, 25%) as yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07132421B2
Source datasetuspto-grants-2006_11
ORD IDord-b409d5c049e44fc9b3ee480d00d8fc9b
Source noteuspto-grants-2006_11