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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1658739Generated: October 29, 2026

Hydrochloric Acid → 1-(8-Fluoro-10,11-dihydro-2-methyl-dibenzo[b,f]-thiepin-10-yl)-4-methyl-piperazine

https://huagongshe.com/reaction/1658739

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactant1-MethylpiperazineHCID 53167—
Reactant10-Chloro-8-fluoro-10,11-dihydro-2-methyldibenzo[b,f]thiepinHCID 12275543—
SolventBenzeneHCID 241—
Product1-(8-Fluoro-10,11-dihydro-2-methyl-dibenzo[b,f]-thiepin-10-yl)-4-methyl-piperazineHCID 21449884—

Reaction Steps

75 G. of 10-chloro-8-fluoro-10,11-dihydro-2-methyl-dibenzo[b,f]-thiepin are heated together with 150 ml. of N-methyl-piperazine at 130° for 10 minutes. Thereafter, the mixture is cooled to 40°, mixed with ice, benzene and aqueous sodium hydroxide solution and again mixed well. The benzene phase is acidified with 6N hydrochloric acid and maintained in an ice bath for 30 minutes. The precipitate is filtered, made alkaline with aqueous sodium hydroxide solution and taken up in benzene. The benzene phase is dried over sodium sulfate and evaporated, whereby 1-(8-fluoro-10,11-dihydro-2-methyl-dibenzo[b,f]-thiepin-10-yl)-4-methyl-piperazine is formed and is treated with maleic acid and the corresponding maleate is formed. The maleate has a melting point of 173°-174°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03966737
Source datasetuspto-grants-1976_06
ORD IDord-6493ca6bd6bf49ecbce8da7c5ed00239
Source noteuspto-grants-1976_06