Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1153958Generated: October 26, 2026

Nefazodone → Nefazodone Hydrochloride

https://huagongshe.com/reaction/1153958

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNefazodoneHCID 4449—
ReactantBenzene, (2-bromoethoxy)-HCID 68526—
ReactantSodiumHCID 5360545—
SolventO-XyleneHCID 7237—
ProductNefazodone HydrochlorideHCID 5491130.7%

Reaction Steps

The sodium salt is pulverized, suspended in 200 ml. of xylene and mixed with phenoxyethyl bromide (10.4 g., 0.052 mole) in 20 ml. of xylene. The resulting mixture is refluxed with stirring for a 64 hr. period and the hot reaction mixture filtered. The filtrate is concentrated under reduced pressure and residual material taken up in ether. Insolubles are collected and the ether filtrate concentrated to afford 22.9 g. (94%) of 2-[3-[4-(3-chlorophenyl)-1-piperazinyl]propyl]-5-ethyl-4-(2-phenoxyethyl)-2H-1,2,4-triazol-3(4H)-one as the free base. Purification of the product is carried out by acidifying a solution of the free base in ethanol with ethanolic hydrogen chloride, and crystallization to afford hydrated (0.25 mole) 2-[3-[4-(3-chlorophenyl)-1-piperazinyl]propyl]-5-ethyl-4-(2-phenoxyethyl)-2H-1,2,4-triazol-3(4H)-one hydrochloride, m.p. 175°-177° C. (30.7% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04487773
Source datasetuspto-grants-1984_12
ORD IDord-0ab313554d974c51af90e245d6559d77
Source noteuspto-grants-1984_12