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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2076652Generated: October 26, 2026

Hydrochloric Acid → 3-Isopropyl-4-methoxyphenylacetonitrile

https://huagongshe.com/reaction/2076652

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant3-Bromo-4-methoxyphenylacetonitrileHCID 522655—
ReactantHCID 178418365HCID 178418365—
CatalystZinc bromideHCID 10421208—
SolventTetrahydrofuranHCID 8028—
Product3-Isopropyl-4-methoxyphenylacetonitrileHCID 1091031083.5%

Reaction Conditions

Temperature-78 °C

Reaction Steps

An isopropylmagnesium bromide-0.63M tetrahydrofuran solution (3.2 ml, 2.0 mmol) was added dropwise to a solution of zinc bromide (473 mg, 2.1 mmol) in tetrahydrofuran (2 ml) under ice-cooling. After the mixture was stirred for 15 minutes, the reaction mixture was cooled to −78° C. After 3-bromo-4-methoxybenzyl cyanide (226 mg, 1.0 mmol) and [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium (II)-dichloromethane adduct (32 mg, 0.04 mmol) were added to the mixture at −78° C., the temperature of the reaction mixture was raised to room temperature and the mixture was further stirred for 5 hours. 1N Hydrochloric acid was added to the reaction mixture and the mixture was extracted with ethyl acetate. The organic layer was successively washed with water and a saturated aqueous NaCl solution and dried with anhydrous sodium sulfate. The residue obtained by removing the solvent under reduced pressure was subjected to silica gel column chromatography (eluting solvent: n-hexane/ethyl acetate=8/1-6/1) to give crude (3-isopropyl-4-methoxyphenyl)acetonitrile (158 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07923573B2
Source datasetuspto-grants-2011_04
ORD IDord-5878e995c9cd44a3ac082cdb4fe373ac
Source noteuspto-grants-2011_04