Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | HCID 23001233 | HCID 23001233 | — |
| Reactant | HCID 23001270 | HCID 23001270 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178478216 | HCID 178478216 | — |
Reaction Steps
A soution of a mixture of 5-[2-(2,4-dichlorophenoxy)benzyloxymethyl]-1-triphenylmethyl-4,5,6,7-tetrahydro-1H-benzimidazole and 5-[2-(2,4-dichlorophenoxy)benzyloxymethyl]-3-triphenylmethyl-4,5,6,7-tetrahydro-3H-benzimidazole (356 mg, 0.55 mmol) in a mixture of glacial acetic acid (9 ml) and water (1 ml) was heated to 70° C. for 2 hours. The reaction mixture was cooled to room temperature. The solvent was removed in vacuo. The crude product was purified by flash chromatography on silica (80 g), using DCM/methanol/−25% aqueous ammonia as eluent, to give 175 mg of the title compound. HPLC method C: elution at 11.42 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06610721B2 |
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| Source dataset | uspto-grants-2003_08 |
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| ORD ID | ord-7b6b6be8f7114166973bef0d56e7f2c6 |
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| Source note | uspto-grants-2003_08 |
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