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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1608581Generated: October 25, 2026

Dichloromethane → 4-Cyano-6,7-dimethyl-1-indanone

https://huagongshe.com/reaction/1608581

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant4-Bromo-6,7-dimethyl-2,3-dihydro-1H-inden-1-oneHCID 13809869—
ReactantHCID 178418546HCID 178418546—
CatalystTrichloroiron;hexahydrateHCID 16211236—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventDimethylformamideHCID 6228—
Product4-Cyano-6,7-dimethyl-1-indanoneHCID 19042293—

Reaction Steps

A mixture of 17.8 g (74.5 mmol) of 4-bromo-6,7-dimethyl-1-indanone [J. Het. Chem. 24, 677 (1987)] and 7.3 g (82 mmol) of copper(I) cyanide in 18 ml of DMF is stirred for 6 hours at 170°. The reaction mixture is then cooled to 100° and 200 ml of toluene and a solution of 31.2 g of iron(III) chloride hexahydrate in 47 ml of water and 8.2 ml of concentrated hydrochloric acid are added in succession thereto. The reaction mixture is stirred for 20 minutes at 70°, cooled and diluted with toluene and water. The organic phase is separated off, washed with water, a semi-saturated sodium hydrogen carbonate solution and again with water, dried and concentrated by evaporation. The residue is crystallised from ethyl acetate and ether and corresponds to starting compound (a). Beige crystals having a melting point of 160°-163° are obtained; IR (CH2Cl2): 2220, 1710 cm-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05395855
Source datasetuspto-grants-1995_03
ORD IDord-055e89f5667443358541f709247e6755
Source noteuspto-grants-1995_03