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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 351562Generated: October 26, 2026

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

https://huagongshe.com/reaction/351562

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 numberUS06743792B2
Source datasetuspto-grants-2004_06
ORD IDord-e22c4e17d82f4d52a1b42abd2bf3c54c
Source noteuspto-grants-2004_06