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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1468586Generated: November 1, 2026

Ethanol → Ethyl N-phenylbenzenecarboximidothioate

https://huagongshe.com/reaction/1468586

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantIodoethaneHCID 6340—
ReactantThiobenzanilideHCID 668263—
ReactantSodium ethoxideHCID 2723922—
SolventDichloromethaneHCID 6344—
ProductEthyl N-phenylbenzenecarboximidothioateHCID 13377974—

Reaction Steps

First, 3.2 g of sodium ethoxide, 10 g of N-phenylthiobenzamide, and 60 mL of ethanol were put in a 300 mL three-neck flask, and stirred at room temperature for 1 hour. Then, 3.7 mL of iodoethane was added to this mixture, and the mixture was heated and stirred at 60° C. for 6 hours to be reacted. After the reaction, ethanol was distilled off under a reduced pressure to give an oily substance. This oily substance was dissolved in dichloromethane, and washed with water and then a saturated aqueous solution of sodium hydrogen carbonate. Then, anhydrous magnesium sulfate was added to the resulting organic layer for drying. The resulting mixture was subjected to gravity filtration, and the filtrate was concentrated, so that N-[(ethylsulfanyl)phenylmethylidene]aniline was prepared (a brown oily substance, crude yield: 110%). The synthesis scheme of Step 1 is shown by (a-1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09005773B2
Source datasetuspto-grants-2015_04
ORD IDord-8fa8d0ea429347b3b77b6350b4ab212f
Source noteuspto-grants-2015_04