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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1414268Generated: October 25, 2026

Diethyl Ether → N-(2-Diethylaminoethyl)-4'-(1-hydroxy-1,2-diphenylbutyl)methanesulfonanilide

https://huagongshe.com/reaction/1414268

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantAmmonium ChlorideHCID 25517—
ReactantN-(2-Diethylaminoethyl)-4'-(1-oxo-2-phenylbutyl)methanesulfonanilideHCID 21486672—
ReactantHCID 178418255HCID 178418255—
SolventWaterHCID 962—
ProductN-(2-Diethylaminoethyl)-4'-(1-hydroxy-1,2-diphenylbutyl)methanesulfonanilideHCID 21486681100%

Reaction Steps

N-(2-Diethylaminoethyl)-4'-(1-oxo-2-phenylbutyl)methanesulfonanilide (24.0 g., 0.0576 mole) is dissolved in 500 ml. ethyl ether and added dropwise during 1/2 hr. to a solution of phenylmagnesium bromide (0.145 mole) in 500 ml. ethyl ether. The mixture is heated at reflux for 16 hrs. After cooling to room temperature, 100 g. of ammonium chloride in 400 ml. water is added and the solution is stirred for 15 min. The ether layer is separated and the aqueous layer is extracted with ethyl ether and the combined ether solutions are washed with water followed by 1N HCl. The acidic aqueous wash is washed with ethyl ether and basified with 50% NaOH to pH 11. The product is extracted with ethyl ether and the ether solution is washed with water and dried (MgSO4). Evaporation of the ethyl ether yields 28 g. of product as an oil (100% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04001229
Source datasetuspto-grants-1977_01
ORD IDord-a92ce907e34b478abedcbe88bd6d492e
Source noteuspto-grants-1977_01