Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl benzoylformate | HCID 15349 | — |
| Reactant | L-Tartaric acid | HCID 444305 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (-)-Ethyl mandelate | HCID 6951556 | — |
Reaction Steps
To a dispersion of 0.43 g (11.3 mmol) of sodium borohydride in THF (35 ml), there was added 1.70 g (11.3 mmol) of L-(+)-tartaric acid, and the mixture was heated under reflux for four hours in an oil bath at 70° C. with stirring. The resulting mixture was cooled in a cryostat at -20° C., a solution of 0.5 g (2.8 mmol) of ethyl phenylglyoxylate in THF (5 ml) was added dropwise over a period of ten minutes, and stirring was continued for 19 hours. The reaction mixture was treated in the same manner as in Example 6, giving 0.44 of ethyl (R)-(-)-2-hydroxy-2-phenylacetate, having a specific rotation [α]D16 of -109° (cl. 00, CHCl3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04943652 |
|---|
| Source dataset | uspto-grants-1990_07 |
|---|
| ORD ID | ord-23d7742559c24a7d8cf6c67f17defabd |
|---|
| Source note | uspto-grants-1990_07 |
|---|