Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2,3-Diaminotoluene | HCID 17593 | — |
| Reactant | Methane, dichloromethoxy- | HCID 21004 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Methylbenzimidazole | HCID 1519341 | 100% |
Reaction Steps
2,3 Diaminotoluene (675 mg, 5.53 mmol) was dissolved in 10 mL of dry tetrahydrofuran and triethylamine (0.77 mL, 5.53 mmol) was added. The mixture was cooled to 0° C. and 1,1-dichloromethyl methyl ether (0.50 mL, 5.53 mmol) was added and the reaction was allowed to warm to room temperature. After 20 hours, the reaction was quenched with sodium bicarbonate. The aqueous phase was extracted with ethyl acetate, dried over magnesium sulfate, filtered and the solvent removed to yield 730 mg (100%) of a brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05212177 |
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| Source dataset | uspto-grants-1993_05 |
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| ORD ID | ord-db7a59d5b616435bbb5f75d38b4a5975 |
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| Source note | uspto-grants-1993_05 |
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