Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | (Diethylamino)sulfur trifluoride | HCID 123472 | — |
| Reactant | 1-(1H-1,3-benzodiazol-2-yl)ethan-1-ol | HCID 205922 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Fluoroethvlbenzimidazole | HCID 53824783 | 38.1% |
Reaction Steps
A solution of 3.24 g (0.02 mole) of 1-hydroxyethylbenzimidazole in 50 ml of methylene chloride was added to a solution of 2.44 ml (0.02 mole) of diethylaminosulfur trifluoride in 50 ml of methylene chloride cooled to -78° C. and under a nitrogen atmosphere. The reaction mixture was allowed to warm slowly to room temperature where it was stirred for 4 hours. The mixture was poured into water, the pH adjusted to 8 with aqueous sodium hydroxide solution and the organic layer separated and dried. Removal of the solvent gave 1.25 g of a brown oil which was chromatographed on 100 g of silica gel using 5% methanol chloroform as the eluent, 845 mg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04782050 |
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| Source dataset | uspto-grants-1988_11 |
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| ORD ID | ord-dd2fc4b3387d4ce39a2ef7faa0ce19b6 |
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| Source note | uspto-grants-1988_11 |
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