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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1454316Generated: October 27, 2026

Triethylamine → 7-Methoxybenzofuran-3-yl trifluoromethanesulfonate

https://huagongshe.com/reaction/1454316

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
Reactant7-Methoxy-2,3-dihydro-1-benzofuran-2-oneHCID 22326942—
SolventDichloromethaneHCID 6344—
Product7-Methoxybenzofuran-3-yl trifluoromethanesulfonateHCID 2082713394.5%

Reaction Steps

To a cold solution (−20° C.) of 3.3 g (20 mmol) 7-methoxy-benzofuranone in 30 mL methylene chloride was added 8.3 mL (6.0 mmol) of triethylamine. To the cold mixture, a solution of 8.5 g (30 mmol) of triflic anhydride in 20 ml of methylene chloride was added dropwise. The temperature was kept at −20° C. or 1 hour. The reaction was then quenched with 100 mL of saturated aqueous sodium bicarbonate aand extracted with methylene chloride (2×150 mL). The combined organic extracts were dried over magnesium sulfate and concentrated in vacuum to give 5.6 g of the desired product. MS (ES) m/z (relative intensity): 265 (M+H,100);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07479500B2
Source datasetuspto-grants-2009_01
ORD IDord-d9b7fbb8ef71437798d00d90073fcbf0
Source noteuspto-grants-2009_01