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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 267915Generated: October 26, 2026

1,2-Dichloroethane → HCID 178423700, compound

https://huagongshe.com/reaction/267915

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantPhenothiazineHCID 7108—
ReactantPotassium HydroxideHCID 14797—
ReactantPhosphorus oxychlorideHCID 24813—
Reactant5-Methyl-2-pyrrolidoneHCID 66055—
ProductHCID 178423700HCID 17842370017%

Reaction Steps

A mixture of 5-methyl-2-pyrrolidinone (6.0 g., 0.06 mole), phosphorus oxychloride (9.2 g., 0.06 mole) in 60 ml. of 1,2-dichloroethane is refluxed for 10 min. A solution of phenothiazine (6.0 g., 0.03 mole) in 20 ml. of 1,2-dichloroethane is added at the end of the reflux period and the reaction mixture stirred and refluxed for 20 hr., and then poured onto 20 ml. of 5N potassium hydroxide and 20 g. of crushed ice. The 1,2-dichloroethane layer is separated and extracted with 30 ml. of 1.5N hydrochloric acid and 30 ml. of water removing water soluble by-product 10-[2-(5-methyl-1-pyrrolinyl)]-phenothiazine hydrochloride. After drying the 1,2-dichloroethane solution over magnesium sulfate, the 1,2-dichloroethane solution is concentrated and the solid thus obtained stirred with 40 ml. of acetone and filtered. Crystallization of the filtercake from ethanol-ether provides analytically pure 10-[5-METHYL-1-(5-METHYL-1 -PYRROLIN-2-YL]PHENOTHIAZINE HYDROCHLORIDE in a yield of 17%, m.p. 257°-264° C. (corr.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03946004
Source datasetuspto-grants-1976_03
ORD IDord-be28f5f9e3d545928b4392e148b1dfae
Source noteuspto-grants-1976_03