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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1583460Generated: October 26, 2026

2,3,4,5,6-Pentafluorobenzyl Alcohol → 4-Methoxy-2,3,5,6-tetrafluorobenzyl alcohol

https://huagongshe.com/reaction/1583460

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3,4,5,6-Pentafluorobenzyl AlcoholHCID 9923—
ReactantSodiumHCID 5360545—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
Product4-Methoxy-2,3,5,6-tetrafluorobenzyl alcoholHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04551546
Source datasetuspto-grants-1985_11
ORD IDord-c2cc50b9b2214ca29e5053cab732dddc
Source noteuspto-grants-1985_11