HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Formate → alpha-Hydroxy-2-nitro-p-tolunitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Formate | HCID 2723810 | — |
| Reactant | 4-(Bromomethyl)-3-nitrobenzonitrile | HCID 21905509 | — |
| Solvent | Water ethanol | HCID 19096565 | — |
| Solvent | Dichloromethane ethylacetate | HCID 21226138 | — |
| Product | alpha-Hydroxy-2-nitro-p-tolunitrile | HCID 17794060 | 77% |
Reaction Steps
A stirred solution containing α-bromo-2-nitro-p-tolunitrile (1.228 g, 5.095 mmol) and sodium formate (0.8664 g, 12.74 mmol) in ethanol:water (4:1, 25 mL) was refluxed for 2 h. The reaction was cooled to room temperature, diluted with 20% CH2Cl2/EtOAc, washed with H2O (3×), dried (MgSO4) and concentrated. Purification by flash chromatography (1,2 and 3% MeOH/CHCl3 gradient) gave 0.695 g (77%) of the title compound as a white solid. 1H NMR (DMSO-d6) δ 4.71 (d, 2H), 5.75 (t, 1H), 7.89 (dd, J=7.9 Hz, 1H), 8.14 (d, J=7.9 Hz, 1H), 8.32 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07132402B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-d906fe819a45423eb4f0dc114dba722f |
| Source note | uspto-grants-2006_11 |