HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → (5-(4-(Trifluoromethoxy)phenyl)pyridin-3-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 5-(4-Trifluoromethoxy-phenyl)-nicotinic acid methyl ester | HCID 58002591 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (5-(4-(Trifluoromethoxy)phenyl)pyridin-3-yl)methanol | HCID 24729847 | 33.6% |
Reaction Steps
A solution of 535 mg (1.76 mmol) 5-(4-Trifluoromethoxy-phenyl)-nicotinic acid methyl ester in 16 ml Ethanol was treated at room temperature (r. t.) with 67 mg (1.76 mmol) of sodium borohydride. The mixture was stirred for 4 h. at r. t., then two days at 80° C. The mixture was poured on ice and extracted tree times with ethyl acetate. The combined organic phases were washed with water, dried (sodium sulphate) and evaporated. Chromatography on silica (eluent: ethyl acetate/methanol 5:1) gave 159 mg (33%) of [5-(4-Trifluoromethoxy-phenyl)-pyridin-3-yl]-methanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07429605B2 |
| Source dataset | uspto-grants-2008_09 |
| ORD ID | ord-d96599b542d2457c84ac0aa46c7c899b |
| Source note | uspto-grants-2008_09 |