HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1755525Generated: October 26, 2026
Toluene → 7-bromo-9,9-dimethyl-N,N-di-p-tolyl-9H-fluoren-2-amine
https://huagongshe.com/reaction/1755525
Participants
| Role | Name | HCID | Charge |
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| Reactant | Toluene | HCID 1140 | — |
| Reactant | Benzenamine, 2-methyl-N-(2-methylphenyl)- | HCID 136423 | — |
| Reactant | 2,7-Dibromo-9,9-dimethylfluorene | HCID 12123876 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+) | HCID 178418228 | — |
| Product | 7-bromo-9,9-dimethyl-N,N-di-p-tolyl-9H-fluoren-2-amine | HCID 86712053 | 66.6% |
Reaction Steps
A mixture of 2,7-dibromo-9,9-dimethyl-9H-fluorene (31.64 g, 89.87 mmol), ditolylamine (8.865 g, 44.9 mmol), Pd(dppf)Cl2 (1.644 g, 2.25 mmol) and sodium tert-butoxide (10.796 g, 112.3 mmol) in toluene 400 mL was degassed and heated at about 80° C. overnight. The resulting mixture was poured into ethyl acetate (500 mL). After the precipitate was filtered off, the solution was washed with water and brine, dried over Na2SO4, loaded on silica gel and purified by flash column (hexane to hexanes/dichloromethane 99:1 to 95:5 gradients). After removal of solvent and recrystallization in dichloromethane/hexanes, a white solid (Compound 32) was obtained (14.0169 g, in 66.6% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09172051B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-dbcc9cdabf984bc6a8ebafc47ca3c079 |
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| Source note | uspto-grants-2015_10 |
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