HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 461778Generated: October 30, 2026
Sodium Hydroxide → HCID 21392455, compound
https://huagongshe.com/reaction/461778
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Bromopinacolone | HCID 21642 | — |
| Reactant | Tetrafluoro-m-phenylenediamine dihydrochloride | HCID 149026 | — |
| Reactant | 4-(2-hydroxyethyl)piperazine-1-carbothioamide | HCID 2051419 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 21392455 | HCID 21392455 | — |
Reaction Steps
5 g of 4-(2-hydroxyethyl)-1-piperazinyl-thiocarboxamide are added to a solution of 3.6 g of bromopinacoline in 70 cc of ethanol, and the reaction mixture is subsequently heated to the boil at reflux for 2 hours. The mixture is then concentrated by evaporation in a vacuum. The residue is dissolved in a small amount of water and is divided between chloroform and a concentrated aqueous sodium hydroxide solution. The chloroform phase is washed with water, dried over sodium sulphate and concentrated by evaporation in a vacuum. Hydrochloric acid in ethanol is added to the resulting oil and the solution is concentrated by evaporation. After recrystallizing the residue from a small amount of ethanol/diethyl ether, 2-[4-(2-hydroxyethyl)-1-piperazinyl]-4-tert.butyl-thiazole dihydrochloride, having a M.P. of 133°-142°, is obtained. The free base is obtained is known manner from the dihydrochloride by treatment with an aqueous sodium hydroxide solution.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04064244 |
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| Source dataset | uspto-grants-1977_12 |
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| ORD ID | ord-95c0f85ddc934d5ab7797455660f17e1 |
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| Source note | uspto-grants-1977_12 |
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