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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1096936Generated: November 1, 2026

Triethylamine → Dimethyl 5-[[(Trifluoromethyl)sulfonyl]oxy]isophthalate

https://huagongshe.com/reaction/1096936

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
Reactant1,3-Benzenedicarboxylic acid, 5-hydroxy-, 1,3-dimethyl esterHCID 83065—
ReactantSodium BicarbonateHCID 516892—
SolventChloroformHCID 6212—
ProductDimethyl 5-[[(Trifluoromethyl)sulfonyl]oxy]isophthalateHCID 10617248—

Reaction Steps

With cooling with ice, trifluoromethanesulfonic acid anhydride (4.04 mL, 24.0 mmol) was added to a mixture of dimethyl 5-hydroxyisophthalate (4.20 g, 20.0 mmol), triethylamine (6.69 mL, 48.0 mmol) and chloroform (40 mL), and stirred for 1 hour with cooling with ice. The reaction mixture was diluted with chloroform, shaken with aqueous saturated sodium hydrogencarbonate solution, then the organic layer was dried with sodium sulfate and concentrated under reduced pressure. The residue was purified through silica gel column chromatography to obtain the title compound as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138197B2
Source datasetuspto-grants-2012_03
ORD IDord-b6b28b53347b4192b3ca7ee000704093
Source noteuspto-grants-2012_03