HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → Ethanol, 2-[(1-methylethyl)(phenylmethyl)amino]-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | Bidisomide | HCID 59798 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Platinum | HCID 23939 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethanol, 2-[(1-methylethyl)(phenylmethyl)amino]- | HCID 11084730 | — |
Reaction Steps
The present invention also relates to a process for preparing α-[2-[acetyl(1-methylethyl)amino]ethyl]-α-(2-chlorophenyl)-1-piperidinebutanamide which has the following formula: ##STR11## and comprises the steps of: (a) alkylating 2-aminoethanol using benzaldehyde and ethanol in the presence of a platinum catalyst and hydrogen followed by reductive alkylation using acetone in the presence of a platinum catalyst and hydrogen to give 2-[(1-methylethyl)(phenylmethyl) amino]ethanol;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05432284 |
| Source dataset | uspto-grants-1995_07 |
| ORD ID | ord-e5a212f1a1d24df68e9d64a90e5033fd |
| Source note | uspto-grants-1995_07 |