HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 539462Generated: October 25, 2026
Diisopropylaniline → HCID 178422447, compound
https://huagongshe.com/reaction/539462
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylaniline | HCID 32484 | — |
| Reactant | 3-Bromo-5-methylbenzonitrile | HCID 14567858 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Reactant | Dichloromethane methanol | HCID 21226129 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 178422447 | HCID 178422447 | — |
Reaction Steps
To a 250 mL 3-neck round bottom flask was added 2,6-diisopropylaniline (2.365 g, 13.34 mmol) and 70 mL toluene. The solution was cooled in an ice bath under nitrogen and trimethylaluminum (2.0 M in toluene, 9.34 mL, 18.68 mmol) was added dropwise via dropping funnel. The reaction mixture was stirred at room temperature for 2 hours. Next, 3-bromo-5-methylbenzonitrile (3.4 g, 17.34 mmol) in 30 mL toluene was added and the reaction mixture was heated to 70° C. overnight under nitrogen. The reaction mixture was cooled in an ice bath and was poured onto a stirring slurry of silica gel in 2:1 dichloromethane/methanol (v/v). The silica gel was filtered off and washed with dichloromethane and methanol. The filtrate was evaporated leaving a solid. Hexane was added to the solvent and the solid was filtered off and washed with hexane (2.92 g, 59%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08871361B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-1d81eecd64a64bf7aca809b9aec5dae4 |
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| Source note | uspto-grants-2014_10 |
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