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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 840775Generated: October 31, 2026

Thionyl Chloride → HCID 70170438, compound

https://huagongshe.com/reaction/840775

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 22620335HCID 22620335—
SolventChloroformHCID 6212—
ProductHCID 70170438HCID 70170438—

Reaction Conditions

Temperature60 °C

Reaction Steps

Thionyl chloride (2 ml) is added to a chloroform solution (30 ml) of 1-(biphenyl-4-ylmethyl)-6-hydroxymethyl-2-methylbenzimidazole (3.62 g), and the solution is stirred for one hour at 60° C. A sodium bicarbonate aqueous solution is added and the reaction is halted. The chloroform layer is washed with water and dried. After removing the solvent through evaporation under reduced pressure, ethyl acetate is added and crystallization is performed. After the crystals are separated through filtration and washed with ethyl acetate, they are dried and thus, 1-(biphenyl-4-ylmethyl)-6-chloro-methyl-2-methylbenzimidazole (2.04 g) is obtained. 1H-NMR (CDCl3, δ): 2.67 (3H, s), 4.71 (2H, s), 5.40 (2H. s), 7.12 (2H, d, J=8.2 Hz), 7.31-7.38 (3H, m), 7.43 (3, s), 7.52-7.58 (4H, m), 7.75 (1H, d, J=8.2 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06369092B1
Source datasetuspto-grants-2002_04
ORD IDord-faa512c2a7e04378b328e76e2f98c42d
Source noteuspto-grants-2002_04