HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 658942Generated: October 30, 2026
1-(5-Fluoro-2-methylphenyl)-3-trimethylsilyoxy-2-aza-1,3-butadiene → HCID 72323512, compound
https://huagongshe.com/reaction/658942
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-(5-Fluoro-2-methylphenyl)-3-trimethylsilyoxy-2-aza-1,3-butadiene | HCID 70178504 | — |
| Reactant | HCID 86647009 | HCID 86647009 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 72323512 | HCID 72323512 | 1.7% |
Reaction Steps
A mixture of E/Z-6-chloro-3-(5-chloro-4-fluoro-2-methoxy-benzylidene)-2-oxo-2,3-dihydro-indole-1-carboxylic acid tert-butyl ester (3 g, 6.8 mmol) and 1-(5-fluoro-2-methyl-phenyl)-3-trimethylsilyoxy-2-aza-1,3-butadiene (30 mmol) prepared in Example 4 in toluene (30 mL) was heated at 60° C. for 3 h, and concentrated in vacuo. To the residue was added DCM (30 mL) and TFA (5 mL), and the resultant solution was stirred at room temperature for 3 h, then concentrated. The residue was partitioned between ethyl acetate and aqueous diluted NaOH solution. The organic layer was washed with water, dried over anhydrous Na2SO4, and concentrated. The residue was purified by flash chromatography to give the title compound as white solid (60 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08076482B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-1ee56cc81a8744f8a551d8811b9d1a27 |
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| Source note | uspto-grants-2011_12 |
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