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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2276997Generated: October 25, 2026

Triethylamine → 5-((E)-2-Ethoxycarbonyl-vinyl)-1H-indole-2-carboxylic acid

https://huagongshe.com/reaction/2276997

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl AcrylateHCID 8821—
ReactantTri-o-tolylphosphineHCID 80271—
Reactant5-Bromo-1H-indole-2-carboxylic acidHCID 252137—
Catalystpalladium(II) acetateHCID 167845—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product5-((E)-2-Ethoxycarbonyl-vinyl)-1H-indole-2-carboxylic acidHCID 5797164586%

Reaction Steps

5-Bromoindole-2-carboxylic acid (400 mg, 1.66 mmol) and tri-O-tolylphosphine (96 mg, 0.32 mmol) were added to a microwave tube. Ethyl acrylate (0.56 ml, 5.6 mmol), Et3N (0.92 ml, 6.6 mmol), acetonitrile (2.5 ml) and Pd(OAc)2 (40 mg, 0.18 mmol) were added. The reaction was placed in a CEM microwave at 150 W, 90° C. for 30 minutes with 5 min ramp time. EtOAc was added and the reaction mixture filtered through celite. The celite pad was washed with DCM and the combined organic fractions removed to give a yellow solid. The solid was redissolved in DCM and extracted into saturated sodium hydrogen carbonate. The aqueous layer was washed with DCM and diethyl ether. The aqueous basic layer was acidified with 2M HCl (pH=5) and the product extracted into EtOAc. The solvent was removed to give the required product (370 mg, 86% yield). LCMS purity 86%, m/z 260 [M++H]+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133104B2
Source datasetuspto-grants-2015_09
ORD IDord-3c26c7c0566b464d95e8408a02b124f6
Source noteuspto-grants-2015_09