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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1072564Generated: November 1, 2026

3,4-Dichlorobenzyl chloride → HCID 22310865, compound

https://huagongshe.com/reaction/1072564

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-Dichlorobenzyl chlorideHCID 7609—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 4-nitro-1H-indole-2-carboxylateHCID 283173—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventDichloromethaneHCID 6344—
ProductHCID 22310865HCID 2231086578%

Reaction Steps

Sodium hydroxide (3M, 20 ml) was added to a vigorously stirred solution of ethyl 4-nitroindole-2-carboxylate (4 g), 3,4-dichlorobenzyl chloride (4.73 ml) and tetra-n-butylammonium hydrogensulphate (0.2 g) in dichloromethane (60 ml). The reaction was stirred for 48 hours then partitioned between 2M HCl and dichloromethane. Combined organic extracts were dried (MgSO4) and concentrated in vacuo and the residue purified by column chromatography using iso-hexane: 20% ethyl acetate as eluent to give the product as a yellow crystalline solid (5.26 g, 78%); NMR δ (CD3SOCD3) 1.3 (t, 3H), 4.3 (q, 2H), 5.95 (s, 2H), 6.9 (m, 1H), 7.6 (m, 4H), 8.2 (t, 2H); M/z (+) 393.3 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06911465B1
Source datasetuspto-grants-2005_06
ORD IDord-6443e55503fd46ceb9f384eb88118515
Source noteuspto-grants-2005_06