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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1789991Generated: October 29, 2026

Cyclohexanecarbonyl chloride → Cyclohexyl 2-Fluorobenzyl Ketone

https://huagongshe.com/reaction/1789991

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanecarbonyl chlorideHCID 75938—
ReactantHCID 178505630HCID 178505630—
CatalystHCID 178418476HCID 178418476—
ProductCyclohexyl 2-Fluorobenzyl KetoneHCID 22037180—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a mixture of 36 ml of 2-fluorobenzylzinc chloride (0.5 M sol. in tetrahydrofuran) and 0.008 g of dichlorobis(triphenylphosphine)palladium(II) stirred at 0° C. was added dropwise via a syringe 2.14 ml of cyclohexanecarbonyl chloride. Afterwards, the reaction mixture was stirred at r.t. for 4 h, quenched with an aqueous saturated solution of ammonium chloride (25 ml), extracted with 20 ml of EtOAc, which was dried (Na2SO4) and evaporated to dryness in vacuo affording 3.52 g of the title compound as a crude, which could be used in the following step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07071197B2
Source datasetuspto-grants-2006_07
ORD IDord-ee37b3bbe8884342a72654bff4d2cc0e
Source noteuspto-grants-2006_07