HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 328959Generated: October 30, 2026
Potassium Hydroxide → HCID 21440126, compound
https://huagongshe.com/reaction/328959
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | HCID 21440223 | HCID 21440223 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethylene Glycol | HCID 8117 | — |
| Product | HCID 21440126 | HCID 21440126 | — |
Reaction Steps
A mixture of 4-benzoyl-3-benzyloxy-5-nitrobenzoic acid (2.7 g), 98% aqueous hydrazine hydrate (4.5 ml), potassium hydroxide (1.5 g) in water (3.0 ml) and di-ethylene glycol (20 ml) is stirred at about 130° C. for 1 hour. The temperature is then slowly raised to 215° C. allowing volatile material to distil off. The stirring at 215° C. is continued for a further 2-3 hours until the nitrogen evolution has ceased. After cooling and dilution with water (30 ml), the resulting solution is acidified with conc. hydrochloric acid (3 ml). The resulting precipitate is collected by filtration and washed with water. After drying and recrystallization twice from 96% ethanol, 5-amino-4-benzyl-3-benzyloxybenzoic acid is obtained with a melting point of 207.5° -209.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04018794 |
|---|
| Source dataset | uspto-grants-1977_04 |
|---|
| ORD ID | ord-7e44ee2f6bd3435b9d348c62981a5b30 |
|---|
| Source note | uspto-grants-1977_04 |
|---|