HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 607220Generated: October 25, 2026
Triethylamine → 2-(4-Methoxy-phenyl)-vinyl-4-methyl-2-nitro-benzene
https://huagongshe.com/reaction/607220
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Methoxystyrene | HCID 12507 | — |
| Reactant | 4-Bromo-3-nitrotoluene | HCID 79224 | — |
| Catalyst | Tri-o-tolylphosphine | HCID 80271 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(4-Methoxy-phenyl)-vinyl-4-methyl-2-nitro-benzene | HCID 86614623 | 58.4% |
Reaction Steps
To a solution of 1-Bromo-4-methyl-2-nitro-benzene (0.76 g, 3.5 mmol), 1-methoxy-4-vinyl-benzene (0.59 g, 4.4 mmol), triethylamine (0.88 g, 8.8 mmol), tri-o-tolylphosphine (0.022 g) and palladium acetate (0.008 g) in N,N-dimethylformamide (7 mL) was placed in a high-pressure tube and purged with nitrogen for 10 mins. The tube was sealed and heated at 120° C. for 16 hours. The mixture was partitioned with water and ethyl acetate adjusting the pH to 3. The organic layer was washed with brine, dried (sodium sulfate) and filtered through a plug of silica. The filtrate was evaporated under vacuum and the residue was triturated with hexane/ethyl acetate (9:1) to provide the title compound (0.55 g, 58%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07915411B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-b53b5d8c8e4342db9e64c29f22f403e5 |
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| Source note | uspto-grants-2011_03 |
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