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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2215356Generated: October 27, 2026

Water → 3-Methoxy-5-methylphenyl trifluoromethanesulfonate

https://huagongshe.com/reaction/2215356

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
Reactant3-Methoxy-5-MethylphenolHCID 76674—
SolventPyridineHCID 1049—
Product3-Methoxy-5-methylphenyl trifluoromethanesulfonateHCID 2194984397.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

Trifluoromethanesulphonic anhydride (2.02 ml, 12.0 mmol) was added dropwise to a stirred solution of 3-methoxy-5-methylphenol (1.50 g, 10.9 mmol) in pyridine (20 ml) at −20° C. under nitrogen. The reaction was warmed to 0° C., stirred for 90 minutes and re-cooled to −20° C. More trifluoromethanesulphonic anhydride (1.01 ml, 6.00 mmol) was added dropwise. The reaction was allowed to warm to room temperature, stirred for 14 hours and cautiously poured into water (100 ml). The aqueous phase was extracted with ether (150 ml) and the organic phases were washed with water (3×75 ml), 0.2M hydrochloric acid (3×75 ml), 1.0M aqueous sodium carbonate solution (2×75 ml), water (75 ml) and brine (75 ml), dried over magnesium sulphate, filtered and concentrated under reduced pressure to provide the title compound (2.86 g) as a pale brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07109228B2
Source datasetuspto-grants-2006_09
ORD IDord-54646e417e6c4c919e1b15b7369889eb
Source noteuspto-grants-2006_09