HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1471228Generated: October 27, 2026
Dimethyl Sulfate → 2-(2-Bromophenyl)-1-methyl-1H-benzimidazole
https://huagongshe.com/reaction/1471228
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-(2-Bromophenyl)-1H-benzimidazole | HCID 97511 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(2-Bromophenyl)-1-methyl-1H-benzimidazole | HCID 16084893 | 83.6% |
Reaction Steps
To a flask were added 3.3 g 2-(2-bromophenyl)-1H-benzimidazole and 100 ml tetrahydrofuran and the mixture was cooled to 10 C under nitrogen. 0.63 g Sodium hydride were added in portions and the reaction mixture was stirred for 20 minutes. 2.0 g Dimethylsulfate were added and the mixture was heated to 22 C for 30 minutes. The mixture was quenched slowly with 100 ml water, extracted with ethyl acetate and then extracted into a 1M hydrochloric acid solution. The solution was washed with ethyl acetate and then basified with 3M sodium hydroxide. Following extraction with ethyl acetate and solvent removal, the solid was dissolved in a hot mixture of 20 ml hexane with 4 ml 2-propanol. After cooling to 5 C, the product was filtered, washed with hexane and dried giving 2.9 g of a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09011734B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-7bbe9fbfaea1405b97468a3c545a1fa8 |
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| Source note | uspto-grants-2015_04 |
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