HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 410336Generated: November 3, 2026
4-Bromobenzyl bromide → 1-(4-Bromo-benzyl)-3-methyl-1,3-dihydro-benzoimidazol-2-ylideneamine
https://huagongshe.com/reaction/410336
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Bromobenzyl bromide | HCID 68527 | — |
| Reactant | HCID 178481316 | HCID 178481316 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | 1-(4-Bromo-benzyl)-3-methyl-1,3-dihydro-benzoimidazol-2-ylideneamine | HCID 58564966 | 61% |
Reaction Steps
To a solution of 1-methyl-1,3-dihydro-benzoimidazol-2-ylideneamine (0.30 g, 2.04 mmol) in 2-butanone (30 ml) was added 4-bromobenzyl bromide (0.70 g, 2.81 mmol). The reaction was heated to 90° C. where it was stirred for 30 min. After this time, the resulting suspension was cooled to rt and filtered. The collected solids were partitioned between dichloromethane and a saturated solution of NaHCO3 and the mixture was stirred for 10 min. The organic layer was separated and the aqueous phase was extracted with additional dichloromethane. The organic fractions were combined, washed with H2O, dried (Na2SO4), filtered and the filtrate was concentrated under reduced pressure to give 1-(4-bromo-benzyl)-3-methyl-1,3-dihydro-benzoimidazol-2-ylideneamine as a white solid (0.39 g, 61%). HPLC-MS 316, 318 [M+1]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08759520B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-cbc38494ede04e8f8a597965f6860ba8 |
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| Source note | uspto-grants-2014_06 |
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