Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | HCID 21250999 | HCID 21250999 | — |
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Product | HCID 21251011 | HCID 21251011 | 62% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06200991B1 |
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| Source dataset | uspto-grants-2001_03 |
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| ORD ID | ord-a92ad32764fd423ebde7a4596d235764 |
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| Source note | uspto-grants-2001_03 |
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