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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2083756Generated: October 31, 2026

Ethyl Bromide → HCID 20357511, compound

https://huagongshe.com/reaction/2083756

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl BromideHCID 6332—
ReactantAmmonium ChlorideHCID 25517—
Reactant4-chloro-N-methylpiperidineHCID 79342—
Reactant2-Bromo-10-thiaxanthenoneHCID 318101—
ReactantMagnesiumHCID 5462224—
SolventTetrahydrofuranHCID 8028—
ProductHCID 20357511HCID 20357511—

Reaction Steps

To 1.2 l g. (0.05 mol) of magnesium turnings covered by tetrahydrofuran in an Argon atmosphere is added about 0.5 g. of 4-chloro-N-methylpiperidine (from 8.5 g., 0.025 mol of the hydrochloride salt) and a small amount of ethyl bromide. The mixture is heated until the reaction is initiated, the remainder of the chloro compound in about 20 ml. of tetrahydrofuran is added and the mixture is refluxed for four hours. 2-Bromothioxanthone (7.3 g., 0.025 mol) is added and the mixture is refluxed for five hours, and then stirred at room temperature 3 days. The reaction mixture is poured into aqueous ammonium chloride and filtered to give 2-bromo-9(1-methyl-4-piperidyl)thioxanthene-9-ol, m.p. 225.5°-226° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04086350
Source datasetuspto-grants-1978_04
ORD IDord-665fd8c5b1cd425494e5416da5445bd1
Source noteuspto-grants-1978_04