HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → HCID 21492496, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 5-(4-Nitrophenoxy)-salicylic acid | HCID 21492504 | — |
| Reactant | HCID 54317397 | HCID 54317397 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 21492496 | HCID 21492496 | — |
Reaction Steps
71 g of 5-(4-nitrophenoxy)-salicylic acid prepared in accordance with Example 1a were hydrogenated at 90° C/100 atms. in 400 ml of ethanol or methanol in the presence of 2.8 g of Raney nickel. The adsorption of hydrogen ceased after 3 hours at the longest. Following the addition of 100 ml of dimethyl acetamide, the catalyst was separated off under heat, water was added at 100° C until a haze began to form, after which the solution was heated for 20 minutes in the presence of 20 g of active carbon and the free aminophenoxy salicylic acid allowed to crystallise out after filtration, being obtained in a yield of 50 g (79% of the theoretical yield), m.p. 223° - 224° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03996197 |
| Source dataset | uspto-grants-1976_12 |
| ORD ID | ord-3e8d812898c54659b1c2a3843b2d1a2d |
| Source note | uspto-grants-1976_12 |