Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,3-Butadiene | HCID 7845 | — |
| Reactant | HCID 68769313 | HCID 68769313 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 68770669 | HCID 68770669 | — |
Reaction Steps
A 10 mL solution of 1:1 1,3-butadiene in toluene stored at −20° C. and 2-chloro-4-fluoro-β-nitrostyrene (2.0 g, 10 mmol) were added to a pressure tube and sealed. The solution was heated to 110° C. and stirred for three days. The reaction mixture was cooled to room temperature, concentrated and the residue was crystallized from hexanes to give the title compound. 1H NMR (300 MHz, CDCl3) δ ppm 7.23-7.28 (m, 1H), 7.11-7.25 (m, 3H), 6.94-7.01 (m, 1H), 5.73-5.83 (m, 2H), 5.04-5.13 (m, 1H), 3.99-4.08 (m, 1H), 2.71-2.82 (m, 2H), 2.51-2.61 (m, 1H), 2.15-2.26 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07834012B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-65f173634db641edb1e67c200b74ff0e |
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| Source note | uspto-grants-2010_11 |
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