HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 3,4,5-Trihydroxybenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Gallic Acid | HCID 370 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Phosphorus trichloride | HCID 24387 | — |
| Reactant | Benzoic acid, 3,4,5-tris(acetyloxy)- | HCID 95088 | — |
| Reactant | 3,4,5-Triacetoxybenzoyl chloride | HCID 155506 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 3,4,5-Trihydroxybenzamide | HCID 69256 | — |
Reaction Steps
Namely, gallic acid is converted into 3,4,5-triacetoxybenzoic acid by reacting with acetic anhydride or acetic acid chloride in the presence of a base such as NaOH (J. Chem. Soc., 2495 (1931)), Na2CO3, pyridine or so on and, further, converted into the corresponding acid chloride by reacting with thionyl chloride or phosphorus trichloride. The thus-obtained 3,4,5-triacetoxybenzoic acid chloride was made to react with an appropriate amine in the presence of a base such as pyridine, triethylamine or the like. Thereafter, the reaction product is treated with sodium acetate, sodium hydroxide or hydrochloric acid in methanol or ethanol to produce an intended gallic acid amide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04476219 |
| Source dataset | uspto-grants-1984_10 |
| ORD ID | ord-cdde5cb78ea24ee3b3a1e264077d2e68 |
| Source note | uspto-grants-1984_10 |