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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2307919Generated: November 1, 2026

3,4-Dichlorobenzyl chloride → Ethyl 3-formyl-N-(3,4-dichlorobenzyl)indole-2-carboxylate

https://huagongshe.com/reaction/2307919

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-Dichlorobenzyl chlorideHCID 7609—
ReactantSodium hydrideHCID 24758—
Reactantethyl 3-formyl-1H-indole-2-carboxylateHCID 5107764—
SolventDimethylformamideHCID 6228—
ProductEthyl 3-formyl-N-(3,4-dichlorobenzyl)indole-2-carboxylateHCID 2260342757%

Reaction Steps

Sodium hydride (488 mg, 60% in mineral oil) was added to a stirred solution of ethyl 3-formylindole-2-carboxylate (2.21 g) in DMF (100 ml) under argon, and reaction stirred at ambient temperature for 25 minutes. 3,4-Dichlorobenzyl chloride (1.71 ml) was then added and the reaction stirred overnight. The reaction mixture was concentrated in vacuo and the residue dissolved in ethyl acetate (80 ml) and washed with water (2×80 ml), dried (MgSO4) and concentrated in vacuo to give a crude residue which was purified by column chromatography using ethyl acetate:iso-hexane as eluent (gradient 5/95-100/0), to give the product as a yellow solid (2.17 g, 57%); NMR d (CD3SOCD3) 1.25 (t, 3H), 4.40 (q, 2H), 5.80 (s, 2H), 7.00 (m, 1H), 7.30-7.50 (m, 3H), 7.55 (m, 1H), 7.65 (m, 1H), 8.35 (m, 1H), 10.48 (s, 1H); M/z (+) 376.4 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06833387B1
Source datasetuspto-grants-2004_12
ORD IDord-b0b33f07078e4f5a94fc9e0bb5194042
Source noteuspto-grants-2004_12