HuagongsheHuagongshe Chemistry Print Report · For research reference only
Salicyl Alcohol → [2-(4'-Trifluoromethylbiphenyl-4-ylmethoxy)phenyl]methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Salicyl Alcohol | HCID 5146 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(4-Trifluoromethylphenyl)benzylchloride | HCID 11459921 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | [2-(4'-Trifluoromethylbiphenyl-4-ylmethoxy)phenyl]methanol | HCID 57864370 | 89.1% |
Reaction Steps
A solution of 4.59 g (36.94 mmol) of 2-hydroxybenzyl alcohol in 200 ml of dry acetonitrile is mixed with 10 g (36.94 mmol) of 4-chloromethyl-4′-trifluoromethylbiphenyl from Example 23A and 6.13 g (44.33 mmol) of anhydrous potassium carbonate and heated to reflux for 12 hours. The mixture is then concentrated to dryness. The residue is taken up in ethyl acetate, washed with water and saturated sodium chloride solution and dried over sodium sulfate. The resulting organic phase is concentrated. The crude product is purified by flash chromatography on silica gel (mobile phase: cyclohexane/ethyl acetate 5:1). 11.8 g (32.92 mmol, 89% yield) of a solid are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07998988B2 |
| Source dataset | uspto-grants-2011_08 |
| ORD ID | ord-f156c46a1d504beeb504970a7234d69a |
| Source note | uspto-grants-2011_08 |