HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrabutylammonium Fluoride → 4-{4-(Benzyloxy)-3-[(4-fluorophenyl)sulphonyl]benzyl}-3,5-dimethylphenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | (4-{4-(Benzyloxy)-3-[(4-fluorophenyl)sulphonyl]benzyl}-3,5-dimethylphenoxy)(triisopropyl)silane | HCID 23499604 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | 4-{4-(Benzyloxy)-3-[(4-fluorophenyl)sulphonyl]benzyl}-3,5-dimethylphenol | HCID 23499617 | — |
Reaction Steps
600 mg (9.95 mmol) of (4-{4-(benzyloxy)-3-[(4-fluorophenyl)sulphonyl]benzyl}-3,5-dimethylphenoxy)-(triisopropyl)silane (Example IX) are dissolved in 15 ml of dichloroethane. At room temperature, 359 mg (1.14 mmol) of tetrabutylammonium fluoride are added, and the mixture is stirred for thirty minutes. The solvent is then removed under reduced pressure and the product is purified by silica gel chromatography (mobile phase cyclohexane/ethyl acetate 9:1). This gives 180 mg (40% of theory) of 4-{4-(benzyloxy)-3-[(4-fluorophenyl)sulphonyl]benzyl}-3,5-dimethylphenol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06777442B2 |
| Source dataset | uspto-grants-2004_08 |
| ORD ID | ord-a20c0f5bd5a043ed806a7f27710858db |
| Source note | uspto-grants-2004_08 |