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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2065907Generated: November 1, 2026

Triethylamine → 3-(4-Cyano-2-ethyl-6-methylphenyl)propionic acid tert-butyl ester

https://huagongshe.com/reaction/2065907

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTrifluoroacetic anhydrideHCID 9845—
Reactant3-(4-Carbamoyl-2-ethyl-6-methylphenyl)propionic acid tert-butyl esterHCID 68553165—
SolventDichloromethaneHCID 6344—
Product3-(4-Cyano-2-ethyl-6-methylphenyl)propionic acid tert-butyl esterHCID 68550351100.9%

Reaction Steps

To a solution of 3-(4-carbamoyl-2-ethyl-6-methyl-phenyl)-propionic acid tert-butyl ester (30.0 g, 103 mmol) and NEt3 (31.3 g, 309 mmol) in DCM (300 mL), trifluoroacetic anhydride (23.8 g, 113 mmol) is added slowly. The exothermic reaction is kept below 5° C. with cooling. After complete addition, the mixture is stirred at rt for 1 h. The mixture is washed twice with water (2×300 mL) and the org. extract is evaporated to dryness to give 3-(4-cyano-2-ethyl-6-methyl-phenyl)-propionic acid tert-butyl ester (28.4 g) as a pale yellow oil; 1H NMR δ 1.25 (t, J=7.5 Hz, 3H), 1.48 (s, 9H), 2.32-2.37 (m, 2H), 2.38 (s, 3H), 2.70 (q, J=7.5 Hz, 2H), 2.95-3.02 (m, 2H), 7.30 (s, 1H), 7.34 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288554B2
Source datasetuspto-grants-2012_10
ORD IDord-6761aefcf18d4259a374d3f0cd619238
Source noteuspto-grants-2012_10