Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 4-[3-(4-Fluorophenyl)propanoyl]benzonitrile | HCID 21843575 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 21843582 | HCID 21843582 | — |
Reaction Steps
1-(4-cyanophenyl)-3-(4-fluorophenyl)-1-propanone (6.35 g, 25 mmol) is dissolved in methanol (50 ml). Sodium borohydride (0.48 g, 12.6 mmol) is added and the mixture is stirred in 30° C. for 1 h. The mixture is rendered acidic with 2M hydrochloric acid and the solvent is evaporated. The residue is dissolved into ethyl acetate. The solution is washed with dilute sodium hydroxide and water, dried and the solvent is evaporated. The product is used for the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05962495 |
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| Source dataset | uspto-grants-1999_10 |
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| ORD ID | ord-e0dd8863189f4261aee43a0a263eefc2 |
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| Source note | uspto-grants-1999_10 |
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