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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1280627Generated: October 26, 2026

Water → ethyl (2RS)-2-acetylamino-3-(3-cyanophenyl)propanoate

https://huagongshe.com/reaction/1280627

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDimethylformamideHCID 6228—
ReactantLithium iodideHCID 66321—
ReactantEthyl 2-acetylamino-2-(3-cyanobenzyl)malonateHCID 22747914—
SolventCyclohexane ethylacetateHCID 21867204—
Productethyl (2RS)-2-acetylamino-3-(3-cyanophenyl)propanoateHCID 85797672—

Reaction Conditions

Temperature150 °C

Reaction Steps

The process is performed as in Example 5, starting with 14.9 g of ethyl 2-acetylamino-2-(3-cyanobenzyl)malonate, 30 g of anhydrous lithium iodide and 150 cm3 of dry dimethylformamide. After stirring for 5 hours at a temperature in the region of 150° C., the reaction mass is cooled to room temperature. 1500 cm2 of water are added and the mixture is extracted with 3 times 300 cm3 of ethyl acetate. The extracts are combined, dried over magnesium sulfate, filtered and concentrated under reduced pressure (5 kPa) at a temperature in the region of 45° C. After drying in an oven at a temperature in the region of 40° C. under reduced pressure (10 Pa), 11.39 g of ethyl (2RS)-2-acetylamino-3-(3-cyanophenyl)propanoate are obtained in the form of a beige-colored paste. (Rf=0.51 in a 90/10 by volume mixture of ethyl acetate/cyclohexane, on a Merck 60F254R silica plate)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06451821B1
Source datasetuspto-grants-2002_09
ORD IDord-eaf4561c059a401ba4f1d331d8dd07df
Source noteuspto-grants-2002_09