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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482787Generated: October 25, 2026

Nefazodone → Nefazodone Hydrochloride

https://huagongshe.com/reaction/482787

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 numberUS04575555
Source datasetuspto-grants-1986_03
ORD IDord-b87a59b3c9564f8aacedc74b1ae53c34
Source noteuspto-grants-1986_03