Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1161842Generated: October 29, 2026

Ammonium Chloride → 4-(3,4-Dimethoxyphenyl)-2,2-dimethyl-4-oxobutanoic acid

https://huagongshe.com/reaction/1161842

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantBenzene, 4-bromo-1,2-dimethoxy-HCID 76114—
Reactant2,2-Dimethylsuccinic anhydrideHCID 87067—
ReactantMagnesiumHCID 5462224—
SolventTetrahydrofuranHCID 8028—
Product4-(3,4-Dimethoxyphenyl)-2,2-dimethyl-4-oxobutanoic acidHCID 24727256—

Reaction Steps

Under an atmosphere of dry nitrogen a grignard solution, prepared from 43.4 g 3,4-dimethoxybromo-benzene and 6.1 g magnesium in 200 ml of tetrahydrofuran, is added dropwise to a solution of 20.5 g 3,3-dimethyl-dihydro-furan-2,5-dione in 200 ml of tetrahydrofuran cooled in an ice-bath. The reaction mixture is stirred for an additional hour at RT. 100 ml of a 20% ammonium chloride solution is added and the water layer is extracted twice with 75 ml of ethyl acetate. The combined organic layers are washed twice with 100 ml of half saturated brine and extracted with 3×100 ml 1M sodium hydroxide solution. The aqueous layers are washed with 75 ml of ethyl acetate, acidified with concentrated hydrochloric acid and extracted 3 times with 100 ml of dichloromethane. The organic layers are dried over magnesium sulfate, filtered and concentrated in vacuo. The oily residue is crystallized from ethyl acetate/petroleum ether (60-80° C.). M. p. 114-116° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820669B2
Source datasetuspto-grants-2010_10
ORD IDord-b38753c06a6948a6ac2437720ff336d9
Source noteuspto-grants-2010_10