HuagongsheHuagongshe Chemistry Print Report · For research reference only
m-Formylbenzonitrile → 3-(Hydroxymethyl)benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | m-Formylbenzonitrile | HCID 90670 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | MeOH tetrahydrofuran | HCID 21899815 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | 3-(Hydroxymethyl)benzonitrile | HCID 2734677 | 98% |
Reaction Steps
To an ice-cold solution of 3-cyanobenzaldehyde (5.0 g, 38 mmol) in 1:1 MeOH/THF (90 mL) was added NaBH4 (1.6 g, 42 mmol), and the reaction mixture was stirred for 3 h. The reaction mixture was diluted with brine, and the solvent was removed under reduced pressure. The residue was dissolved in water, and the aqueous layer was extracted with Et2O (3×100 mL). The combined organics were washed with brine, dried (MgSO4), filtered, and concentrated under reduced pressure to provide 3-hydroxymethyl-benzonitrile (4.95 g, 98%) as a clear oil, which was used in the next step without further purification or characterization.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07067540B2 |
| Source dataset | uspto-grants-2006_06 |
| ORD ID | ord-83c13575ba8b4df2984304d092f5b4e4 |
| Source note | uspto-grants-2006_06 |