HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → {3-Methyl-5-[5-(trifluoromethyl)pyridin-2-yl]thien-2-yl}methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 3-Methyl-5-[5-(trifluoromethyl)pyridin-2-yl]thiophene-2-carbaldehyde | HCID 21986306 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | {3-Methyl-5-[5-(trifluoromethyl)pyridin-2-yl]thien-2-yl}methanol | HCID 21986475 | — |
Reaction Steps
A mixture of 3-methyl-5-[5-(trifluoromethyl)pyridin-2-yl]thiophene-2-carbaldehyde (intermediate 78, 0.144 g) in tetrahydrofuran (10 ml) and water (15 ml) was treated with sodium borohydride (0.03 g). The reaction was stirred at room temperature for 30 minutes, extracted with ethyl acetate and the organic layer washed with water and dried with brine and over magnesium sulfate. The title compound was isolated after removal of the desiccant and evaporation of the solvent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07091237B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-c4c7b667259941398d24acbf3497c507 |
| Source note | uspto-grants-2006_08 |