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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1582633Generated: October 30, 2026

Potassium Carbonate → Ethyl 5-acetoxy-N-(3,4-dichlorobenzyl)indole-2-carboxylate

https://huagongshe.com/reaction/1582633

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-(Bromomethyl)-1,2-dichlorobenzeneHCID 639726—
ReactantEthyl 5-acetoxyindole-2-carboxylateHCID 11379620—
SolventAcetonitrileHCID 6342—
ProductEthyl 5-acetoxy-N-(3,4-dichlorobenzyl)indole-2-carboxylateHCID 1146388163%

Reaction Conditions

Temperature80 °C

Reaction Steps

3,4-Dichlorobenzyl bromide (5.96 g) was added to a stirred solution of ethyl 5-acetoxyindole-2-carboxylate (5.4 g) and potassium carbonate (6.94 g) in acetonitrile (500 ml) under an atmosphere of argon. The reaction was heated at 80° C. for 16 hours, then concentrated in vacuo and the residue partitioned between ethyl acetate and water. Combined organic extracts were washed with water, saturated aqueous sodium chloride and dried. The solvent was removed in vacuo and the residue was triturated with iso-hexane to yield the product as a cream solid (5.55 g, 63%). NMR: δ 1.27 (t, 3H), 2.27 (s, 3H), 4.28 (q, 2H), 5.82 (s, 2H), 6.90 (d, 1H), 7.09 (dd, 1H), 7.33-7.40 (m, 2H), 7.46 (d, 1H) 7.52 (d, 1H), 7.60 (d, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06737435B1
Source datasetuspto-grants-2004_05
ORD IDord-638c2b903ab74bd990ab98626ca2372b
Source noteuspto-grants-2004_05