HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → (4-(4-Chloro-3-(trifluoromethyl)phenoxy)phenyl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 4-(4-Chloro-3-(trifluoromethyl)phenoxy)benzaldehyde | HCID 86666187 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (4-(4-Chloro-3-(trifluoromethyl)phenoxy)phenyl)methanol | HCID 66825563 | 79.1% |
Reaction Steps
To a solution of 4-{[4-chloro-3-(trifluoromethyl)phenyl]oxy}benzaldehyde (21 g, 69.8 mmol) in methanol (200 mL) was added slowly NaBH4 (2.64 g, 69.8 mmol) portionwise. The mixture was stirred at room temperature overnight. After removing the solvent, the residue diluted with DCM. The resulting suspension was filtered, the filtrate was concentrated in vacuo to afford the title compound (17.6 g, 55.2 mmol, 79% yield) as yellow solid. LCMS: rt=1.71 min, [M+H+]=303, 305
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08637536B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-ba06b45cef644bfba7ae761a3b7e6f36 |
| Source note | uspto-grants-2014_01 |