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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1188511Generated: October 26, 2026

Sulfuryl chloride → 4-Chloro-5-(methyloxy)-2-(trifluoromethyl)-1H-benzimidazole

https://huagongshe.com/reaction/1188511

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuryl chlorideHCID 24648—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178488085HCID 178488085—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product4-Chloro-5-(methyloxy)-2-(trifluoromethyl)-1H-benzimidazoleHCID 5780029480.2%

Reaction Steps

Sulfuryl chloride (0.39 mL, 4.86 mmol) was added dropwise to a 0° C. solution of 5-(methyloxy)-2-(trifluoromethyl)-1H-benzimidazole (1.0 g, 4.63 mmol) in HOAc (10 mL). The ice bath was removed and the mixture was allowed to stir at rt for 2 h. The concentrated reaction mixture was suspended in a mixture of EtOAc and H2O and the pH was adjusted to 7 with saturated aqueous NaHCO3. The reaction was partitioned and the aqueous portion was extracted with EtOAc. The combined organic fractions were washed with brine, dried (Na2SO4), filtered, and concentrated in vacuo to afford the title compound (0.93 g): MS (ESI) m/z 251 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673948B2
Source datasetuspto-grants-2014_03
ORD IDord-e722d31834a44acd828b9010d4cfb0ce
Source noteuspto-grants-2014_03