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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2220214Generated: November 1, 2026

Triethylamine → Methyl 5-formyl-2-(trifluoromethylsulfonyloxy)benzoate

https://huagongshe.com/reaction/2220214

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAmmonium ChlorideHCID 25517—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
ReactantMethyl 5-FormylsalicylateHCID 14363598—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductMethyl 5-formyl-2-(trifluoromethylsulfonyloxy)benzoateHCID 1546684976%

Reaction Steps

To a solution of 5-formyl-2-hydroxy-benzoic acid methyl ester (1.0 g, 5.6 mmol) in CH2Cl2 (10 mL) at −78° C. was added Et3N (0.85 mL, 6.1 mmol) and DMAP (68 mg, 0.56 mmol) followed by dropwise addition of Tf2O (1.03 mL, 6.1 mmol) over 20 min. The reaction mixture was then warmed to room temperature and poured into saturated aqueous NH4Cl and extracted with CH2Cl2 (3×25 mL). The combined extracts were dried (Na2SO4), filtered and concentrated. The residue was purified by flash chromatography (SiO2, 15% EtOAc/hexanes) to afford Example 236A (1.3 g, 76%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07417040B2
Source datasetuspto-grants-2008_08
ORD IDord-dae4071e38364b91b8339e3847150321
Source noteuspto-grants-2008_08