HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium → 2,6-Bis(trifluoromethyl)benzenemethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | Potassium | HCID 5462222 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | Methyl 2,6-bis(trifluoromethyl)benzoate | HCID 22420073 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2,6-Bis(trifluoromethyl)benzenemethanol | HCID 15346431 | 94.1% |
Reaction Steps
58 ml of a 1.2M solution of diisobutylaluminium hydride (DIBAH) were added at 0° C. to a solution of 5.59 g of the product of Stage A and 60 ml of toluene. The temperature was allowed to return to 20° C. and the reaction mixture was stirred for 4 hours, then poured into a molar solution of potassium and sodium double tartrate and extracted with isopropyl ether. The aqueous phase was saturated with sodium chloride, followed by extraction with ethyl acetate, drying, filtering, rinsing and bringing to dryness to obtain after chromatography on silica (eluant: hexane-ethyl acetate (9-1)), 4.72 g of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05504112 |
| Source dataset | uspto-grants-1996_04 |
| ORD ID | ord-85784df3dd1b437eb489df32cab2f0c6 |
| Source note | uspto-grants-1996_04 |