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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1576172Generated: October 25, 2026

3-Methylbenzaldehyde → m-Ethylbenzaldehyde

https://huagongshe.com/reaction/1576172

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-MethylbenzaldehydeHCID 12105—
Reactant{[2-(Methoxycarbonyl)phenyl]methyl}(triphenyl)phosphanium bromideHCID 10743695—
Reactant3'-Methylstilbene-2-carboxylic acidHCID 53685216—
SolventAcetonitrileHCID 6342—
Productm-EthylbenzaldehydeHCID 118623—
Product3'-Ethylstilbene-2-carboxylic acidHCID 53663434—

Reaction Steps

116.5 Gm. of 1,5-diazobicyclo[3.4.0]nonene-5 is added to 107.5 gm. of m-tolualdehyde and 400 gm. of o-carbomethoxybenzyltriphenylphosphonium bromide in 2000 ml. of acetonitrile. The mixture is refluxed briefly then cooled and the solvent removed under vacuum. The residue is dissolved in chloroform and washed with dilute hydrochloric acid, and the solution dried and evaporated. The product is refluxed for 11 hours in a solution of 111 gm. potassium hydroxide in 1000 ml. of water and 150 ml. of methanol. The solution is cooled and extracted with chloroform. The aqueous solution is acidified with concentrated hydrochloric acid and extracted with chloroform. The extract is dried and evaporated to give 177.5 gm. (91%) of 3'-methylstilbene-2-carboxylic acid (ca. 60:40 cis:trans). Use of m-ethylbenzaldehyde instead of m-tolualdehyde gives a similar yield of 3'-ethylstilbene-2-carboxylic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03979430
Source datasetuspto-grants-1976_09
ORD IDord-757c2cf4506c49e4a946ae130899d353
Source noteuspto-grants-1976_09