HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 3-(Methylthio)-5-(trifluoromethyl)benzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Triacetoxyperiodinane | HCID 159087 | — |
| Reactant | [3-(Methylthio)-5-(trifluoromethyl)phenyl]methanol | HCID 68687257 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(Methylthio)-5-(trifluoromethyl)benzaldehyde | HCID 59343879 | — |
Reaction Steps
A solution of [3-(methylthio)-5-(trifluoromethyl)phenyl]methanol (200 mg, 0.99 mmol) in CH2Cl2 (20 mL) was cooled to 0° C. and then Dess-Martin periodinane (573 mg, 1.35 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 (75 mL). The organic extracts were washed with brine (25 mL), dried over Na2SO4, filtered, and concentrated. Purification by flash chromatography with 1% to 10% EtOAc/hexanes afforded 3-(methylthio)-5-(trifluoromethyl)benzaldehyde. Rf=0.55 (25% EtOAc/hexanes). 1H NMR (CDCl3, 500 MHz) δ 10.02 (s, 1H), 7.87 (s, 1H), 7.84 (s, 1H), 7.68 (s, 1H), 2.58 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07737295B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-ee6070e3ae2143b68083edc55242dab9 |
| Source note | uspto-grants-2010_06 |