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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1487846Generated: October 31, 2026

Chlorosuccinimide → Methyl 3-(5-chloro-2-methyl-1H-imidazol-4-yl)-4-methylbenzoate

https://huagongshe.com/reaction/1487846

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
ReactantMethyl 4-methyl-3-(2-methyl-1H-imidazol-5-yl)benzoateHCID 90029434—
SolventCarbon TetrachlorideHCID 5943—
ProductMethyl 3-(5-chloro-2-methyl-1H-imidazol-4-yl)-4-methylbenzoateHCID 9003015882.1%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of methyl 4-methyl-3-(2-methyl-1H-imidazol-5-yl)benzoate (compound 7.1, 317 mg, 1.38 mmol) in carbon tetrachloride (30 mL) was added NCS (184 mg, 1.38 mmol). The mixture was stirred at 50° C. for 16 hours, then cooled to room temperature and washed with brine, dried (MgSO4), filtered, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (0-50% EtOAc in hexanes) to yield the title compound as a solid (300 mg, 82%). m/z (ES+) 265 (M+H)+. 1H NMR (400 MHz, CDCl3) δ 9.55 (br s, 1H), 8.01-7.87 (m, 2H), 7.37 (d, J=7.8 Hz, 1H), 3.91 (s, 3H), 2.42 (s, 3H), 2.40 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09428502B2
Source datasetuspto-grants-2016_08
ORD IDord-c447fe4b4e78465189f50041ebc33696
Source noteuspto-grants-2016_08