Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Anthranilamide | HCID 6942 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | HCID 20338676 | HCID 20338676 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 65884-03-9 | HCID 3050173 | — |
Reaction Steps
A mixture of 75 g. 2-aminobenzamide, 138 g. sodium acetate, 174 g. 1-(2-chloropropyl)-4-phenylpiperazine dihydrochloride, and 455 ml. water was refluxed 4 hours and left overnight at room temperature. Chloroform (200 ml.) was added, the mixture stirred, then filtered. The solid was washed with chloroform which dissolved most of it. The chloroform was separated, the aqueous layer washed with chloroform. The combined chloroform extracts were washed with water, dried, and concentrated to dryness. The residue was recrystallized from 1800 ml. ethanol and again from 2200 ml. ethanol to give 26.3 g., m. 197-8° . A 3rd recrystallization from 1600 ml. ethanol gave 22.4 g. m. 196-8.5° . A 10 g. portion of this was suspended in 100 ml. 95% ethanol, heated to near reflux and 15 ml. 10% hydrochloric acid added. The mixture was cooled with stirring and the solid filtered, washed with ethanol, and dried over P2O5 under vacuum to give 10.8 g., m. 274-81° (dec.)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04060526 |
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| Source dataset | uspto-grants-1977_11 |
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| ORD ID | ord-25616fef822c42079f5580ad725146c4 |
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| Source note | uspto-grants-1977_11 |
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