HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium borohydride → 2-(4-Bromo-2-methyl-phenyl)-4-hydroxy-butyronitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | 3-(4-Bromo-2-methyl-phenyl)-3-cyano-propionic acid methyl ester | HCID 66877131 | — |
| Reactant | KHSO4 Na2SO4 | HCID 86586342 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(4-Bromo-2-methyl-phenyl)-4-hydroxy-butyronitrile | HCID 59428334 | 87% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
Lithium borohydride (4.99 g, 0.2290 mol) was added to a room temperature solution of 3-(4-bromo-2-methyl-phenyl)-3-cyano-propionic acid methyl ester (43.08 g, 0.1527 mol) in THF (500 mL) and the reaction mixture was stirred overnight. The reaction mixture was cooled to 0° C., and a solution of 10% KHSO4/Na2SO4 was slowly added until pH 1-2 was reached. The resulting mixture was extracted with EtOAc, and the combined organic extracts were washed with water and brine, dried over Na2SO4, filtered, and evaporated under reduced pressure. The residue was purified via flash chromatography (hexane/EtOAc, 7/3) to give 27.3 g (87% yield) of 2-(4-bromo-2-methyl-phenyl)-4-hydroxy-butyronitrile as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07776910B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-9e7375483a8e47399aedbb2bb604d1d2 |
| Source note | uspto-grants-2010_08 |