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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 461094Generated: October 31, 2026

4-Methoxybenzaldehyde → Ethyl 3-hydroxy-3-(4-methoxyphenyl)-2-methylpropanoate

https://huagongshe.com/reaction/461094

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethoxybenzaldehydeHCID 31244—
ReactantEthyl 2-bromopropionateHCID 79040—
CatalystZincHCID 23994—
SolventBenzeneHCID 241—
SolventDiethyl EtherHCID 3283—
ProductEthyl 3-hydroxy-3-(4-methoxyphenyl)-2-methylpropanoateHCID 312882—

Reaction Steps

To 36.2 g (0.55 mole) of purified zinc dust is added portionwise a solution of 80 g p-anisaldehyde (0.58 mole) in 80 ml of anhydrous benzene, 20 ml anhydrous ether and 98 g (0.54 mole) of ethyl 2-bromopropionate from a separatory funnel. About 15 ml of this solution is added to the zinc and the flask is warmed until the reaction starts and then heating is removed and allowed to continue exothermally. The addition takes about an hour. The reaction mixture is refluxed for 40 minutes and then cooled in an ice bath and hydrolyzed by the addition of 250 ml of cold 10% sulfuric acid with vigorous stirring. The acid layer is drawn off and the benzene solution is extracted twice with 63 ml of 5% sulfuric acid followed by 30 ml of 10% sodium carbonate solution, then with 3 × 30 ml of 5% sulfuric acid, and finally with 2 × 30 ml of water. The combined acid solution is extracted with 2 × 100 ml of ether and the combined ether and benzene solution is washed with 2 × 50 ml of saturated sodium chloride, then it is dried over sodium sulfate for 11/2 hours and filtered. Most of the solvent is removed on an evaporator. The rest is distilled under vacuum to obtain ethyl β-(p-methoxyphenyl)-β-hydroxy-α-methylpropionate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04061771
Source datasetuspto-grants-1977_12
ORD IDord-89565c730d6d49a096755637e9c898d1
Source noteuspto-grants-1977_12