HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 19934850, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Methyl 2-(2,6-dimethyl-4-formylphenoxy)-2-(3-chlorophenyl)acetate | HCID 18950590 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 19934850 | HCID 19934850 | 63% |
Reaction Steps
To a solution of 1.260 g (3.79 mmol) of the product of Step A in 8 mL methanol was added 0.072 g (1.90 mmol) of sodium borohydride and the reaction mixture was stirred at room temperature for 15 minutes. Excess borohydride was quenched with water, and the reaction mixture was extracted into EtOAc. The organic layer was dried (MgSO4), filtered, evaporated, and then purified on a silica gel flash chromatography column eluted with 30% EtOAc-hexane. The purified fractions were combined, evaporated and dried in vacuo to afford 0.790 g (63%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05374638 |
| Source dataset | uspto-grants-1994_12 |
| ORD ID | ord-c3747f79d2f642da9692d4d8e3c71bda |
| Source note | uspto-grants-1994_12 |