HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium borohydride → 2-Hydroxy-4-(hydroxymethyl)benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | Methyl 4-cyano-3-hydroxybenzoate | HCID 16641129 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Hydroxy-4-(hydroxymethyl)benzonitrile | HCID 21696974 | — |
Reaction Steps
Methyl 4-cyano-3-hydroxybenzoate, as described in Example 4, Step C, (0.50 g, 2.82 mmol) was dissolved in dry THF (30 mL), treated with LiBH4 (2.0M solution in THF) (5.64 mL, 11.28 mmol) and heated at reflux overnight. The reaction mixture was concentrated, then partitioned between EtOAc (50 mL) and 1N HCl (50 mL). Next, the aqueous layer was extracted with additional EtOAc (2×50 mL), the organic layers were combined, washed with brine, and dried (MgSO4). The title compounds was obtained by filtering and concentrating to dryness.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06297239B1 |
| Source dataset | uspto-grants-2001_10 |
| ORD ID | ord-cfc0a830161845479db49df7ee137ff5 |
| Source note | uspto-grants-2001_10 |