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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522150Generated: October 27, 2026

Trifluoromethanesulfonic acid → HCID 118497051, compound

https://huagongshe.com/reaction/522150

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoromethanesulfonic acidHCID 62406—
ReactantN-bromobutanimideHCID 67184—
Reactant2-Chloro-4-hydroxy-benzoic acid methyl esterHCID 13498830—
SolventAcetonitrileHCID 6342—
ProductHCID 118497051HCID 11849705137%

Reaction Steps

A solution of methyl 2-chloro-4-hydroxybenzoate (5.0 g, 26.8 mmol) in MeCN (100 mL) was cooled to −30° C. Triflic acid (2.60 mL, 29.48 mmol) was added followed by N-bromosuccinimide (5.25 g, 29.48 mmol) and the reaction was warmed to room temperature and stirred for 1.5 hours. The reaction was quenched by the addition of saturated aqueous Na2CO3 solution (50 mL). The solution was extracted with EtOAc (2×100 mL), the combined organic layers were combined, dried over magnesium sulphate and concentrated in vacuo. The residue was purified by silica gel column chromatography eluting with 20-40% EtOAc in heptanes to afford the title compound as a white solid (2.60 g, 37%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09328096B2
Source datasetuspto-grants-2016_05
ORD IDord-1a487335e1d149d6934cc481fab7c867
Source noteuspto-grants-2016_05