HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 2-Fluoro-4-(3-hydroxy-1-propyl)benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 18536111 | HCID 18536111 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Fluoro-4-(3-hydroxy-1-propyl)benzonitrile | HCID 18536071 | — |
Reaction Steps
To a solution of the product from Step C (140 mg, 0.71 mmol) in 3.5 mL of ethanol at 0° C. was added sodium borohydride (84 mg, 2.1 mmol). After 45 minutes, another portion of sodium borohydride was added, and the mixture was stirred overnight. The reaction was quenched with saturated NH4Cl solution, concentrated in vacuo, and partitioned between EtOAc and saturated NaHCO3 solution. The organic layer was washed with brine, dried (Na2SO4), filtered, and concentrated in vacuo to provide the alcohol which was sufficiently pure for use in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06562823B1 |
| Source dataset | uspto-grants-2003_05 |
| ORD ID | ord-4ac9113e3c274ce586405de51822ba11 |
| Source note | uspto-grants-2003_05 |