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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1272511Generated: November 3, 2026

Methane → 6-(3-Chloro-4-fluorobenzoyl)-1-oxa-6-azaspiro[2.5]octane-2-carbonitrile

https://huagongshe.com/reaction/1272511

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
ReactantChloroacetonitrileHCID 7856—
ReactantN-(3-chloro-4-fluorobenzoyl)-piperidine-4-oneHCID 10611056—
CatalystTetrabutylammonium ChlorideHCID 70681—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventSodium HydroxideHCID 14798—
Product6-(3-Chloro-4-fluorobenzoyl)-1-oxa-6-azaspiro[2.5]octane-2-carbonitrileHCID 12043633—

Reaction Conditions

Temperature15 °C

Reaction Steps

A suspension of 1-(3-chloro-4-fluorobenzoyl)piperidin-4-one (4160 g, 16.27 mol) in 28.4 liters of dichloromethane and 11.7 liters of sodium hydroxide at 30.5%, supplemented with 186 g of tetrabutylammonium chloride, is cooled to 15° C. Chloroacetonitrile (1540 ml, 24.4 mol) is then added slowly and with vigorous stirring and the mixture is stirred for 3 hours at 20° C. Further addition of chloroacetonitrile (500 ml) is carried out in order to complete the reaction. The reaction medium is diluted with dichloromethane (8.5 liters) and water (20 liters) and then separated by decantation and washed again with water. The brown solution obtained is decolorized with 2 kg of silica and 500 g of animal charcoal and then evaporated to dryness. The residue obtained is crystallized from isopropanol in order to give, after filtration, 3426 g of brown crystals. m.p.=100–101° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07208603B2
Source datasetuspto-grants-2007_04
ORD IDord-da48c8f1b19f419eb41a2cb3005a31a4
Source noteuspto-grants-2007_04