HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → (2,3-Difluoro-4-methylphenyl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | Tert-butyl-(2,3-difluoro-4-methyl-benzyloxy)-dimethyl-silane | HCID 18550272 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2,3-Difluoro-4-methylphenyl)methanol | HCID 2774146 | — |
Reaction Steps
To a solution of tert-butyl-(2,3-difluoro-4-methyl-benzyloxy)-dimethyl-silane (6.5 g, 24 mmol) in THF (24 mL) was added tetrabutylammonium fluoride (24 mL of a 1M solution in THF, 24 mmol). After stirring at ambient temperature for 1 hour, the mixture was poured into water, acidified with 1M aqueous HCl, extracted 3× with ethyl acetate, and the combined organic layers were dried over Na2SO4, filtered and concentrated in vacuo. The residue was purified by silica gel chromatography (10:1 to 2:1 hexane-ethyl acetate), affording (2,3-Difluoro-4-methyl-phenyl)-methanol as a light yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07405218B2 |
| Source dataset | uspto-grants-2008_07 |
| ORD ID | ord-7056f7698a2d450c85404e2fd4a5bd09 |
| Source note | uspto-grants-2008_07 |