HuagongsheHuagongshe Chemistry Print Report · For research reference only
Amino-alpha-ethyl-benzhydrol → 3-Amino-alpha-ethyl-benzhydrol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Amino-alpha-ethyl-benzhydrol | HCID 2803285 | — |
| Reactant | HCID 20324253 | HCID 20324253 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Potassium Hydroxide | HCID 14797 | — |
| Product | 3-Amino-alpha-ethyl-benzhydrol | HCID 20324259 | — |
Reaction Steps
2.6 g. of 3-amino-4-chloro-α-ethyl-benzhydrol are dissolved in methanol containing 3.9 g of potassium hydroxide. 8.7 g. of an 5% palladium-on-calcium carbonate catalyst are added to the mixture, and the suspension is hydrogenated at room temperature under atmospheric pressure. After the uptake of the calculated amount of hydrogen the catalyst is filtered off and washed with 15 ml. of methanol. The filtrate and the wash are combined and concentrated to 40 ml. under reduced pressure. The product is precipitated from the concentrate with water. The solids are filtered off, washed until neutral, and dried until constant weight. The crude product is recrystallized from alcohol to yield 1.7 g. of 3 amino-α-ethyl-benzhydrol, melting at 92-93° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04094908 |
| Source dataset | uspto-grants-1978_06 |
| ORD ID | ord-aa9bd2ae660a4af89b8c740503bc79b0 |
| Source note | uspto-grants-1978_06 |