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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2307916Generated: November 1, 2026

3,4-Dichlorobenzyl chloride → Methyl N-(3,4-dichlorobenzyl)-2-methoxycarbonyl-3-indoleacetate

https://huagongshe.com/reaction/2307916

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-Dichlorobenzyl chlorideHCID 7609—
ReactantPotassium CarbonateHCID 11430—
Reactantmethyl 3-(2-methoxy-2-oxoethyl)-1H-indole-2-carboxylateHCID 10332197—
SolventAcetonitrileHCID 6342—
ProductMethyl N-(3,4-dichlorobenzyl)-2-methoxycarbonyl-3-indoleacetateHCID 5437067365.1%

Reaction Conditions

Temperature80 °C

Reaction Steps

3,4-Dichlorobenzyl chloride (8.2 g) was added to a stirred solution of methyl 2-methoxycarbonyl-3-indoleacetate (6.5 g) and potassium carbonate (8.36 g) in acetonitrile (200 ml) under an atmosphere of argon. The reaction was heated to 80° C. for 24 hours. The reaction was concentrated in vacuo and partitioned between ethyl acetate and water. Combined organic extracts were washed with saturated aqueous sodium chloride solution, dried (MgSO4) and concentrated in vacuo. The residue was purified by column chromatography using 25% ethyl acetate:iso-hexane as eluent to give the product as a white solid (6.95 g, 65%), NMR d (CD3SOCD3) 3.60 (s, 3H), 3.77 (s, 3H), 4.13 (s, 2H), 5.89 (s, 2H), 6.89 (dd, 1H), 7.16 (t, 1H), 7.27 (d, 1H), 7.34 (t, 1H), 7.52 (d, 1H), 7.57 (d, 1H), 7.78 (d, 1H); M/z (+) 406 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06833387B1
Source datasetuspto-grants-2004_12
ORD IDord-3cf926484c394417b443da5113a6b4e4
Source noteuspto-grants-2004_12