HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1975286Generated: October 29, 2026
Hydrochloric Acid → 3-(3-Aminopropyl)benzamide
https://huagongshe.com/reaction/1975286
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | N-[3-(3-carbamoylphenyl)propyl]phthalimide | HCID 19377229 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-(3-Aminopropyl)benzamide | HCID 19377231 | 47.7% |
Reaction Steps
A mixture of 15.42 g (0.05 mole) N-[3-(3-carbamoylphenyl)propyl]phthalimide (the product of step (e)), 2.76 g (0.055 mole) hydrazine monohydrate and 100 ml ethanol was refluxed for about four hours under argon with heat, and then allowed to stir overnight. The reaction mixture was acidified with 30% (v/v) hydrochloric acid to a pH of about 1. Additional ethanol (about 10 to 20 ml) was added to the thick mixture. The mixture was filtered; the solids were rinsed with ethanol. The filtrate was evaporated to give a solid. Water (about 15 ml) was added to the solid; the resulting mixture was filtered. The filtrate wa basified with dry potassium carbonate until saturated, then extracted three times with 20 ml butanol. The butanol extracts were dried over sodium sulfate and potassium carbonate overnight, filtered and stripped to give 4.25 g of the above-identified product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05286252 |
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| Source dataset | uspto-grants-1994_02 |
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| ORD ID | ord-70a006006f77445b8dc480960ec19ed3 |
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| Source note | uspto-grants-1994_02 |
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