HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 22449944, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 22449933 | HCID 22449933 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Formaldehyde | HCID 712 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 22449944 | HCID 22449944 | — |
Reaction Steps
To a solution of 3.5 g of (+) threo 1-(p-nitrophenyl)-2-(4-benzylpiperidin-1-yl)-1-aminopropan-1-ol in 35 ml of ethanol and 9 ml of 2 M hydrochloric acid and 5 ml of formaldehyde 40% solution was added portionwise 1.1 g or sodiumcyanoborohydride. After stirring 1 h, the solution was diluted with ethylacetate and basified with a concentrated ammonium hydroxide solution. The organic phase was dried and the solvent removed, affording 3.8 g of (+) threo 1-(p-nitro-phenyl)-2- (4-benzylpiperidin-1-yl) -3-dimethylaminopropan-1-ol, m.p. 132-135° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06407122B1 |
| Source dataset | uspto-grants-2002_06 |
| ORD ID | ord-848e6600c69c499c99c19476495ed181 |
| Source note | uspto-grants-2002_06 |