HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 5-(Hydroxymethyl)-2-(3-(trifluoromethyl)phenoxy)benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Benzonitrile, 5-formyl-2-[3-(trifluoromethyl)phenoxy]- | HCID 86666203 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-(Hydroxymethyl)-2-(3-(trifluoromethyl)phenoxy)benzonitrile | HCID 66825436 | 89.5% |
Reaction Steps
A mixture of 5-formyl-2-{[3-(trifluoromethyl)phenyl]oxy}benzonitrile (1 g, 3.43 mmol) and NaBH4 (0.156 g, 4.12 mmol) in ethanol (20 mL) was stirred at room temperature for 3 h. The reaction was quenched with NH4Cl saturated solution and extracted with EA. The organic layer was separated and concentrated to afford the title compound (0.9 g, 89% yield) as a white solid. LCMS: rt=3.71 min
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08637536B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-d0af28bef8084da08b622990ca47483a |
| Source note | uspto-grants-2014_01 |