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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1096950Generated: October 31, 2026

Pyridine → Methyl 5-{[(trifluoromethyl)sulfonyl]oxy}biphenyl-3-carboxylate

https://huagongshe.com/reaction/1096950

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAmmonium ChlorideHCID 25517—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
ReactantMethyl 3-hydroxy-5-phenylbenzoateHCID 18945322—
SolventChloroformHCID 6212—
ProductMethyl 5-{[(trifluoromethyl)sulfonyl]oxy}biphenyl-3-carboxylateHCID 57930914—

Reaction Steps

With cooling with ice, pyridine (1.2 mL) and trifluoromethanesulfonic acid anhydride (1.2 mL) were added to a CHCl3 (40 mL) solution of methyl 5-hydroxybiphenyl-3-carboxylate, and stirred for 30 minutes with cooling with ice. Aqueous ammonium chloride was added to the reaction liquid, extracted with ethyl acetate, and the organic layer was washed with water, aqueous saturated sodium bicarbonate solution and saturated saline water. This was dried with anhydrous sodium sulfate, filtered and concentrated under reduced pressure to obtain the title compound as a yellow oil. Not purified, this was used in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138197B2
Source datasetuspto-grants-2012_03
ORD IDord-c681af8e231949be8797ae88eb495444
Source noteuspto-grants-2012_03