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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1387146Generated: November 1, 2026

Diethyl Ether → HCID 178520539, compound

https://huagongshe.com/reaction/1387146

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 11474387HCID 11474387—
ReactantHCID 178418471HCID 178418471—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178520539HCID 178520539—

Reaction Steps

5 mmol of 4-(1-(triphenylmethyl)imidazol-4-yl)butanenitrile are introduced into a solution of 3-phenylpropylmagnesium bromide in 300 ml of diethyl ether and 100 ml of tetrahydrofuran and the mixture is brought to reflux for 6 h. Hydrolysis is carried out with an ammonium chloride solution, the organic phase is separated and the aqueous phase is stirred with dichloromethane. The combined and concentrated organic phases are brought to boiling point for 2 h in a 2N aqueous/alcohol (ethanol/water) hydrochloric acid solution. The ethanol is removed under vacuum, filtration is carried out and basification is carried out. The title compound is stirred in dichloromethane and recrystallized in the hydrogenmaleate form from ethanol/diethyl ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE037303E1
Source datasetuspto-grants-2001_07
ORD IDord-ca96e31034284ac49c7dbe30d134ba29
Source noteuspto-grants-2001_07