HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(Aminomethyl)Benzoic Acid → HCID 178511262, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(Aminomethyl)Benzoic Acid | HCID 65526 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Reactant | HCID 178511261 | HCID 178511261 | — |
| Catalyst | Ruthenium | HCID 23950 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 178511262 | HCID 178511262 | — |
Reaction Steps
Trans-4-aminomethylcyclohexane-1-carboxylic acid was prepared using 30 g of p-aminomethylbenzoic acid, 3 g of 5% ruthenium supported on activated carbon and 300 ml of 14N hydrochloric acid or a 20% aqueous sodium hydroxide solution as a solvent under the conditions shown in Table 2 below. For the purposes of comparison, the results obtained by isomerizing 100% cis-4-aminomethylcyclohexane-1-carboxylic acid under the same conditions as above but without using hydrogen for reduction are also shown in Table 2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04048222 |
| Source dataset | uspto-grants-1977_09 |
| ORD ID | ord-c9e4722ef0d64534a1a2f8ac742257c6 |
| Source note | uspto-grants-1977_09 |