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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1531838Generated: November 2, 2026

Chloroform → HCID 21251011, compound

https://huagongshe.com/reaction/1531838

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantHCID 21250999HCID 21250999—
ReactantPotassium hydroxy sulfiteHCID 23707502—
ProductHCID 21251011HCID 2125101162%

Reaction Conditions

Temperature0 °C

Reaction Steps

3.8 g of previously moistened alumina, 7.07 g (11.5 mmol) of oxone and 10 ml of chloroform are vigorously stirred. A solution of 0.9 g (3.7 mmol) of 1-phenyl-2-methylthio-4,5,6,7-tetrahydro-1H-benzimidazole, solubilized in 10 ml of chloroform, is added to this medium and then the stirring is continued while heating under reflux for 2 hours. The mixture is cooled to 0° C. and then filtered, the solid is rinsed with 10 ml of chloroform and 10 ml of a 9/1 THF/CH3OH mixture. The filtrate is concentrated under reduced pressure and then purified on a silica column with the aid of a 99/1 then 98/2 dichloromethane/methanol mixture. 0.65 g of product is obtained. Yield=62%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06200991B1
Source datasetuspto-grants-2001_03
ORD IDord-a92ad32764fd423ebde7a4596d235764
Source noteuspto-grants-2001_03