HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → trans-N-(1,2,3,4-tetrahydro-4-hydroxy-1-naphthyl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | N-(4-Oxo-1,2,3,4-tetrahydronaphthalen-1-yl)acetamide | HCID 13037024 | — |
| Solvent | Water | HCID 962 | — |
| Product | trans-N-(1,2,3,4-tetrahydro-4-hydroxy-1-naphthyl)acetamide | HCID 70619274 | — |
Reaction Steps
A mixture of 19.2 g. of N-(1,2,3,4-tetrahydro-4-oxo-1-naphthyl)acetamide and 275 ml. of absolute ethanol is stirred under a nitrogen atmosphere and 3.58 g. sodium borohydride added. The reaction mixture is stirred at room temperature for 16 hours, then 200 ml. of water is added and the stirring continued for 4 hours. Next, the reaction mixture is evaporated to dryness in vacuo and the residue treated with 250 ml. of water. The mixture is cooled in an ice bath and acidified with concentrated hydrochloric acid. The precipitated yellow solid is collected and dried; weight 6 g., m.p. 120°-127° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04049717 |
| Source dataset | uspto-grants-1977_09 |
| ORD ID | ord-ad9663ffbb4b4764a34ae45b0cf9b3e5 |
| Source note | uspto-grants-1977_09 |