HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 19786582, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 53770206 | HCID 53770206 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ammonium Chloride | HCID 25517 | — |
| Product | HCID 19786582 | HCID 19786582 | 100% |
Reaction Steps
In a 2 liter round-bottomed flask was dissolved 4,5,6,7-tetrahydro-4-oxo-3-phenyl-1,2-benzisoxazol-5-acetic acid ethyl ester (3.0 g) in absolute ethanol (300 ml) at room temperature. Sodium borohydride (6.07 g) was added and the solution was heated to reflux. The solution was cooled to room temperature, then diluted with saturated NH4Cl until a solid appeared. The reaction mixture was basified to pH 9 using 10% NAOH (aq.). The product, an oil, was extracted with ether and the aqueous phase was extracted twice with ether. The combined organic layers were washed with brine, dried (MgSO4), filtered and concentrated to give 2.60 g of 4-hydroxy-5-(2-hydroxyethyl)-3-phenyl-4,5,6,7-tetrahydro-1,2-benzisoxazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05256672 |
| Source dataset | uspto-grants-1993_10 |
| ORD ID | ord-ee67cc65e5a74f9e8a4d304ab1e6c78a |
| Source note | uspto-grants-1993_10 |