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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1971836Generated: October 27, 2026

Trifluoromethanesulfonic anhydride → Trifluoro-methanesulfonic acid 4-fluoro-2-(morpholine-4-sulfonyl)-phenyl ester

https://huagongshe.com/reaction/1971836

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
Reactant4-Fluoro-2-(morpholine-4-sulfonyl)-phenolHCID 58126990—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductTrifluoro-methanesulfonic acid 4-fluoro-2-(morpholine-4-sulfonyl)-phenyl esterHCID 5812702679.5%

Reaction Steps

To a solution of 4-fluoro-2-(morpholinosulfonyl)phenol (0.4 g, 1.5 mmol) and DMAP (0.28 g 2.29 mmol) in CH2Cl2(10 ml), Tf2O (0.93 ml 5.5 mmol) was added dropwise at 0° C. The mixture was stirred at room temperature for 4 h, after which the mixture was washed with hydrochloric acid (1N, 20 ml) and then extracted with EA. The extracts were combined, washed with brine, dried over sodium sulfate and evaporated into dryness. The resulting residue was purified by column chromatography using PE/EA (10/1) as eluent to give the desired product (469 mg, yield 78%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431581B2
Source datasetuspto-grants-2013_04
ORD IDord-800cd6ab29a14f4daacf2d1bd5918ea4
Source noteuspto-grants-2013_04