HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 885085Generated: October 30, 2026
4-Methoxystyrene → HCID 11579752, compound
https://huagongshe.com/reaction/885085
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methoxystyrene | HCID 12507 | — |
| Reactant | 4-Bromo-3-nitroanisole | HCID 79288 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Catalyst | 2-(Di-tert-butylphosphino)biphenyl | HCID 2734215 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 11579752 | HCID 11579752 | 79.2% |
Reaction Steps
To a stirred solution of 2-bromo-5-methoxynitrobenzene (5 g, 21.6 mmol) in dry acetonitrile (60 mL) were added 4-methoxystyrene (3.04 g, 22.6 mmol), N,N-diisopropylethylamine (8.36 g, 64.6 mmol), biphenyl-2-yl-di-t-butyl phosphine (385 mg, 1.3 mmol) and palladium acetate (290 mg, 1.3 mmol). The resulting mixture was heated at 80° C. overnight under N2. The reaction mixture was cooled to room temperature and partitioned between ethyl acetate and water. The organic layer was separated, washed with water, brine, and dried over magnesium sulfate. Concentration under reduced pressure gave the crude product which was purified by column chromatography using ethyl acetate in hexane (5%-10%) to give the protected nitro-stilbene (4.4 g, 72%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08242144B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-0d63bf7393654a1a8136e5fe0fd2b3d5 |
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| Source note | uspto-grants-2012_08 |
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