HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → (4-(Methylsulfonyl)-2-(trifluoromethyl)phenyl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 4-Methanesulfonyl-2-(trifluoromethyl)benzaldehyde | HCID 51342018 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (4-(Methylsulfonyl)-2-(trifluoromethyl)phenyl)methanol | HCID 66936507 | — |
Reaction Steps
To a suspension of 4-methanesulfonyl-2-trifluoromethyl-benzaldehyde (49.2 g, 0.20 mol) in dry EtOH (500 ml), cooled in an ice-bath, is added sodium borohydride (10.8 g, 0.22 mol), portionwise over 30 mins. The reaction mixture is allowed to warm up slowly to room temperature then stirring is continued for 16 h. The reaction mixture is poured into a beaker of crushed ice (700 ml) and adjusted to pH 1 with 2N HCl (approx. 200 ml). The resulting pale yellow suspension is extracted with CH2Cl2 (3×150 ml), dried (MgSO4) and evaporated to dryness in vacuo. to afford a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07888383B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-73aca806d3dc47a1b52b33f1efaadbaf |
| Source note | uspto-grants-2011_02 |