Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1586291Generated: October 27, 2026

Methyl iodide → 2-(3,4-Dimethoxyphenyl)-4,5-dimethoxybenzoic acid

https://huagongshe.com/reaction/1586291

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantNitromethaneHCID 6375—
Reactant2-[2-(3,4-Dimethoxyphenyl)-4,5-dimethoxyphenyl]-4,4-dimethyl-2-oxazolineHCID 21218168—
Product2-(3,4-Dimethoxyphenyl)-4,5-dimethoxybenzoic acidHCID 15428753—

Reaction Steps

2-[2-(3,4-Dimethoxyphenyl)-4,5-dimethoxyphenyl]-4,4-dimethyl-2-oxazoline (10 g) was dissolved in nitromethane (100 ml), to which was added methyl iodide (10 ml), and the mixture was allowed to stand at room temperature for 24 hours. It was concentrated by an evaporator, and methanol (150 ml) and a 20% aqueous sodium hydroxide solution (150 ml) were added to the residue to reflux for 18 hours. The solvent was distilled off until the system becomes ununiform, and water was added until it becomes transparent. After washing with diethyl ether (200 ml), the aqueous layer was cooled in a ice-water bath and concentrated hydrochloric acid was added until it becomes acidic. The insoluble matter formed was filtered, washed with water and dried to give 7.7 g of 2-(3,4-dimethoxyphenyl)-4,5-dimethoxybenzoic acid as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05942641
Source datasetuspto-grants-1999_08
ORD IDord-3ef9d7f5ae7c4712896c5f1980743259
Source noteuspto-grants-1999_08