HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1514864Generated: November 2, 2026
2,6-Dimethylbenzaldehyde → HCID 66965797, compound
https://huagongshe.com/reaction/1514864
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,6-Dimethylbenzaldehyde | HCID 583841 | — |
| Reactant | HCID 66965669 | HCID 66965669 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 66965797 | HCID 66965797 | — |
Reaction Steps
A mixture of 3,4-diamino-N-(3-chloro-phenyl)-benzamide (0.1 mL in 0.2 M DMSO solution), 2,6-dimethyl-benzaldehyde (0.1 mL in 0.2 M toluene solution) and YB(SO3CF3)3 (0.1 mL in 0.02M THF solution) was shaked at room temperature for 16 h. Then another 0.04 mL of 2,6-dimethyl benzaldehyde (0.2 M) toluene solution was added. The mixture was stirred in open air at ambient temperature overnight. The mixture was then diluted by MeOH and the whole was loaded onto a solid phase extraction (SPE) cartridge that contained strong cation exchange (SCX) (1 g media in 6 mL cartridge, United Chemical Technology). Wash-to-waste (5 mL MeOH) was followed by elute-to-collect (5 mL 20:2:1 ethyl acetate-MeOH-Et3N) and, after evaporation of volatiles, the crude was further purified by silica gel column chromatography to give of 2-(2,6-dimethyl-phenyl)-3H-benzoimidazole-5-carboxylic acid (3-chloro-phenyl)-amide as white powder: MS (m/z) 376 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08222248B2 |
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| Source dataset | uspto-grants-2012_07 |
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| ORD ID | ord-a3e5d80eb6d344928bbcbeaee84d8290 |
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| Source note | uspto-grants-2012_07 |
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