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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704183Generated: October 27, 2026

Ethanol → ethyl (2RS)-2-(2-cyano-10-phenothiazinyl)propionate

https://huagongshe.com/reaction/704183

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantEthyl 2-chloropropionateHCID 10807—
ReactantSodium hydrideHCID 24758—
ReactantPhenothiazine-2-carbonitrileHCID 98841—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Productethyl (2RS)-2-(2-cyano-10-phenothiazinyl)propionateHCID 14502135—

Reaction Steps

A solution of 2-phenothiazinecarbonitrile (224.5 g) in dimethylformamide (1 liter) is introduced, with stirring and in the course of 2 hours 30 minutes, into a suspension of sodium hydride (24 g) in dimethylformamide (1 liter) at a temperature in the region of 25° C., and the mixture is left stirred for a further 1 hour 15 minutes until the evolution of gas has ceased. The fine suspension obtained is introduced, with stirring and at a temperature in the region of 25° C., in the course of 4 hours 30 minutes, into a solution of ethyl 2-chloropropionate (255 cc) in dimethylformamide (1 liter), and stirring is continued for 16 hours. Ethanol (100 cc) is then poured into the reaction mixture, and thereafter the whole is poured into a mixture of ice (2 kg) in distilled water (4 liters): a gum precipitates and then crystallizes. The solid formed is drained, washed successively with distilled water (6×500 cc) and petroleum ether (2× 500 cc) and dried in the air. Ethyl (2RS)-2-(2-cyano-10-phenothiazinyl)propionate (296.5 g) is thereby obtained in the form of yellowish brown crystals, m.p. 117°-8° C., which are used as they are in the next stage.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04985419
Source datasetuspto-grants-1991_01
ORD IDord-d48d56b4a7d04dc4a6ee21c3793e13f9
Source noteuspto-grants-1991_01