HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium cyanoborohydride → 3-Phenyl-2-furanmethanamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 3-Phenylfuran-2-carbaldehyde | HCID 13465704 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-Phenyl-2-furanmethanamine | HCID 69129923 | 13.1% |
Reaction Steps
Stir a solution of 3-phenylfuran-2-carbaldehyde (401 mg, 2.33 mmol) and NH4OAc (1.79 g, 23.30 mmol) in methanol (8 mL) at room temperature under nitrogen. Add NaCNBH3 (102 mg, 1.63 mmol). After stirring at room temperature for 24 hours, concentrate the mixture, dilute with water (2 mL), basify with 1N sodium hydroxide, and extract with diethyl ether (4×10 mL). Dry the combined organic phases (magnesium sulfate), filter and concentrate. Perform flash chromatography on silica gel eluting with 9:1 ethyl acetate/MeOH to afford 37 mg of the title compound as a yellow solid. 1H NMR (CDCl3) δ 7.19-7.41 (m, 6H), 6.49 (d, J=2 Hz, 1H), 3.95(s, 2H), 1.80 (br s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07265246B2 |
| Source dataset | uspto-grants-2007_09 |
| ORD ID | ord-04b5727dfaa54c1e9c06cb272af8238e |
| Source note | uspto-grants-2007_09 |