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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 462079Generated: October 27, 2026

2-Chlorophenothiazine → 2-Chloro-10-propargylphenothiazine

https://huagongshe.com/reaction/462079

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChlorophenothiazineHCID 7088—
ReactantPropargyl bromideHCID 7842—
ReactantButyllithiumHCID 178418339—
ReactantHCID 178506919HCID 178506919—
SolventDiethyl EtherHCID 3283—
Product2-Chloro-10-propargylphenothiazineHCID 14959696—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution containing 0.2 mole of butyllithium in 350 ml. of absolute ether (prepared in situ under nitrogen) were added 46.5 g. (0.2 mole) of 2-chlorophenothiazine while the mixture was maintained at -10° C. The reaction mixture was then allowed to stir for forty-five minutes at 0° C. To the resulting solution of 2-chloro-10-phenothiazinyllithium were added 30 g. (0.25 mole) of propargyl bromide in 30 ml. of absolute ether. This reaction mixture was allowed to stir at room temperature overnight. After quenching with dilute hydrochloric acid, the ethereal phase of the reaction mixture was washed with water and dried over anhydrous calcium sulfate. Upon removal of the solvent a semi-solid mass of crude 2-chloro-10-propargylphenothiazine remained. Recrystallized from methanol and from ether-hexane, pure 2-chloro-10-propargylphenothiazine melted at 112.0°-115.0° C. The structure was confirmed by nuclear magnetic resonance spectroscopy.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04065471
Source datasetuspto-grants-1977_12
ORD IDord-b3a745db87544f81be1cbaee1a99296f
Source noteuspto-grants-1977_12