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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1758915Generated: October 26, 2026

Nefazodone → Nefazodone Hydrochloride

https://huagongshe.com/reaction/1758915

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 numberUS04338317
Source datasetuspto-grants-1982_07
ORD IDord-c1bd14cd830d4878a974d498d8b07cc5
Source noteuspto-grants-1982_07