HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 267915Generated: October 26, 2026
1,2-Dichloroethane → HCID 178423700, compound
https://huagongshe.com/reaction/267915
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Phenothiazine | HCID 7108 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 5-Methyl-2-pyrrolidone | HCID 66055 | — |
| Product | HCID 178423700 | HCID 178423700 | 17% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03946004 |
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| Source dataset | uspto-grants-1976_03 |
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| ORD ID | ord-be28f5f9e3d545928b4392e148b1dfae |
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| Source note | uspto-grants-1976_03 |
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