HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 3-Nitro-5-(trifluoromethyl)benzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Triacetoxyperiodinane | HCID 159087 | — |
| Reactant | (3-Nitro-5-(trifluoromethyl)phenyl)methanol | HCID 18621888 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Nitro-5-(trifluoromethyl)benzaldehyde | HCID 53404039 | — |
Reaction Steps
A solution of [3-nitro-5-(trifluoromethyl)phenyl]methanol (400 mg, 1.88 mmol) in CH2Cl2 (20 mL) was cooled to 0° C. and then Dess-Martin periodinane (1.59 g, 3.76 mmol) was added. The reaction was slowly warmed to room temperature. After stirring at room temperature for twenty minutes, the reaction was poured into 1N NaOH (25 mL). The mixture was extracted with EtOAc (50 mL) and the organic extracts were washed with brine (25 mL), dried over Na2SO4, filtered, and concentrated. Purification by flash chromatography with 0% to 15% EtOAc/hexanes afforded 3-nitro-5-(trifluoromethyl)benzaldehyde. Rf=0.39 (15% EtOAc/hexanes). 1H NMR (CDCl3, 500 MHz) δ 10.18 (s, 1H), 8.91 (s, 1H), 8.74 (s, 1H), 8.48 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07737295B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-be7a8636429c40c3998dcd62c31e2409 |
| Source note | uspto-grants-2010_06 |