HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,3,4,5,6-Pentafluorobenzyl Alcohol → 4-Methoxy-2,3,5,6-tetrafluorobenzyl alcohol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,3,4,5,6-Pentafluorobenzyl Alcohol | HCID 9923 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-Methoxy-2,3,5,6-tetrafluorobenzyl alcohol | HCID 11961895 | — |
Reaction Steps
Pentafluorobenzyl alcohol (1.98 g) was added to a stirred solution of sodium methoxide (obtained by dissolving sodium (0.4 g) in methyl alcohol (10 ml) at the ambient temperature, and the mixture heated at the reflux temperature for 3.5 hours. After cooling the mixture, the solvent was removed by evaporation under reduced pressure and the residue partitioned between water and diethyl ether. After separating the ethereal layer and washing with water, it was dried over anhydrous magnesium sulphate and concentrated by evaporation of the solvent under reduced pressure to yield 4-methoxy-2,3,5,6-tetrafluorobenzyl alcohol (1.8 g), identical with the product of Example 5.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04551546 |
| Source dataset | uspto-grants-1985_11 |
| ORD ID | ord-c2cc50b9b2214ca29e5053cab732dddc |
| Source note | uspto-grants-1985_11 |