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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 463708Generated: October 30, 2026

(3,4-Dimethoxyphenyl)acetic acid → 2-(3,4-Dimethoxyphenyl)-3-{{[(3,4-dimethoxyphenyl)methyl]carbonyl}amino}propanoic acid ethyl ester

https://huagongshe.com/reaction/463708

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3,4-Dimethoxyphenyl)acetic acidHCID 7139—
ReactantSodium HydroxideHCID 14798—
ReactantThionyl ChlorideHCID 24386—
Reactant(3,4-Dimethoxyphenyl)acetyl chlorideHCID 3604458—
ReactantHCID 69551005HCID 69551005—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
Product2-(3,4-Dimethoxyphenyl)-3-{{[(3,4-dimethoxyphenyl)methyl]carbonyl}amino}propanoic acid ethyl esterHCID 13560525—

Reaction Steps

A mixture of 289 g of alpha-(aminomethyl)-3,4-dimethoxybenzeneacetic acid ethyl ester hydrochloride, 1000 ml of methylene chloride and 1000 ml of water was cooled to 0° and adjusted to pH 9.0 with 4N sodium hydroxide. A solution of 1000 ml of methylene chloride and 3,4-dimethoxyphenyl acetic acid chloride [previously prepared by the action of 400 ml of thionyl chloride on 215 g of 3,4-dimethoxyphenyl acetic acid in 500 ml of toluene at 50° for 1 hour and evaporation to dryness] was added concurrently with 4N sodium hydroxide maintaining a pH of 7.0-8.0. Upon completion of the acid chloride addition, the pH was maintained at 9.0 for 1 hour followed by acidification to pH 1.0 with 6N hydrochloric acid. The layers were separated and the aqueous layer extracted once with methylene chloride. The combined organic layers were washed once with excess saturated sodium bicarbonate solution, dried over sodium sulfate and evaporated in vacuo to give 430 g of 2-(3,4-dimethoxyphenyl)-3-{{[(3,4-dimethoxyphenyl)methyl]carbonyl}amino}propanoic acid ethyl ester as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04544657
Source datasetuspto-grants-1985_10
ORD IDord-35d47ebdff3e4476a21a56f8a62db778
Source noteuspto-grants-1985_10