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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 965636Generated: October 25, 2026

Hydrochloric Acid → (+/-)-alpha-(3,4-Dichlorophenyl)-2,6-dimethyl-4-nitrobenzeneacetonitrile

https://huagongshe.com/reaction/965636

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium hydrideHCID 24758—
Reactant(3,4-Dichlorophenyl)acetonitrileHCID 76690—
Reactant2-Methoxy-1,3-dimethyl-5-nitrobenzeneHCID 139835—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product(+/-)-alpha-(3,4-Dichlorophenyl)-2,6-dimethyl-4-nitrobenzeneacetonitrileHCID 2231292687%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of (3,4-dichlorophenyl)acetonitrile (0.149 mol) in DMF (100 ml) was stirred at 0° C. under N2 flow. Sodium hydride (0.223 mol) was added portionwise. The mixture was stirred at 0° C. under N2 flow for 1 hour. A mixture of, 2-methoxy-1,3-dimethyl-5-nitrobenzene (0.149 mol) in DMF (100 ml) was added dropwise at 0° C. under N2 flow. The mixture was stirred at RT for 6 hours, then cooled, hydrolized with H2O and with HCl 3N and extracted with EtOAc. The organic layer was separated, washed several times with H2O, dried, filtered and the solvent was evaporated. The residue was crystallized from DIPE. The precipitate was filtered off and dried, yielding 43.4 g (87%) of (±)-α-(3,4-dichlorophenyl)-2,6-dimethyl-4-nitrobenzeneacetonitrile (interm. 48).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06951857B2
Source datasetuspto-grants-2005_10
ORD IDord-d08b914b289c4b42965af605431dc2e3
Source noteuspto-grants-2005_10