HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → (4-(4-Chloro-2-fluorophenyl)-2-methylpyridin-3-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 4-(4-Chloro-2-fluorophenyl)-2-methylnicotinaldehyde | HCID 86695950 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (4-(4-Chloro-2-fluorophenyl)-2-methylpyridin-3-yl)methanol | HCID 86695951 | 248.3% |
Reaction Steps
To a solution of 4-(4-chloro-2-fluorophenyl)-2-methylnicotinaldehyde (60 mg, 0.240 mmol) in MeOH (2 mL) at 0° C., was added NaBH4 (27.3 mg, 0.721 mmol) and the solution stirred for 3 h at RT. The mixture was concentrated and diluted with EtOAc (15 mL) and water (10 mL). The organic layers were dried over Na2SO4, filtered and concentrated under reduced pressure to afford (4-(4-chloro-2-fluorophenyl)-2-methylpyridin-3-yl)methanol (0.15 g, 0.596 mmol, 89% yield) as a brown solid. LCMS (ESI) m/e 252.03 [(M+H)+, calcd for C13H12ClFNO 252.1]; LC/MS retention time (Method G): tR=0.80 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08703953B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-9e71eb39df304392918df5b2da984f91 |
| Source note | uspto-grants-2014_04 |