HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 5803-73-6
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | ethyl 2-oxo-2-(5,6,7,8-tetrahydronaphthalen-2-yl)acetate | HCID 13368011 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5803-73-6 | HCID 13368014 | 99.1% |
Reaction Steps
A solution of sodium borohydride (2.0 g) in ethanol (100 ml) was added dropwise to an ice-cooled solution of ethyl 5,6,7,8-tetrahydro-2-naphthylglyoxylate (34.5 g) in ethanol (200 ml). After completion of dropwise addition, acetic acid (6 ml) was added and the reaction mixture was poured into water and extracted with chloroform. The chloroform layer was washed with water, dried (MgSO4) and the solvent was distilled off to give ethyl 2-hydroxy-(5,6,7,8-tetrahydro-2-naphthyl)acetate (34.5 g, yield 9%) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05071841 |
| Source dataset | uspto-grants-1991_12 |
| ORD ID | ord-4355ff7e551e4432a8519ed6de275ebd |
| Source note | uspto-grants-1991_12 |