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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1421771Generated: October 26, 2026

Triethylamine → Methyl 3-Cyano-4-(trifluoromethylsulfonyloxy)benzoate

https://huagongshe.com/reaction/1421771

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
ReactantSodium BicarbonateHCID 516892—
ReactantMethyl 3-cyano-4-hydroxybenzoateHCID 11769089—
SolventDichloromethaneHCID 6344—
ProductMethyl 3-Cyano-4-(trifluoromethylsulfonyloxy)benzoateHCID 53821226—

Reaction Conditions

Temperature0 °C

Reaction Steps

3-cyano-4-hydroxybenzoic acid methyl ester from example 51, step 1 (2 g, 11.3 mmol) was dissolved in CH2Cl2 (57 ml) and cooled to 0° C. in an ice bath. The mixture was treated with Et3N (3 ml, 22.6 mmol) followed by the addition of Tf2O (1.9 ml, 11.3 mmol). The reaction mixture was warmed to room temp. and stirred for 4 hours. Saturated NaHCO3 (10 mL) was added and the mixture was extracted with EtOAc (2×10 mL). The organic layers were combined and dried (MgSO4), filtered, and concentrated. The residue was then purified by flash chromatography (15% EtOAc/Hexane) to yield the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06077853
Source datasetuspto-grants-2000_06
ORD IDord-8434b885ff4f43ae9460551a8ed99495
Source noteuspto-grants-2000_06