Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | Methyl cyanoacetate | HCID 7747 | — |
| Reactant | 1-(4-Fluoro-2-methoxyphenyl)ethan-1-one | HCID 142887 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 67102427 | HCID 67102427 | 95.6% |
Reaction Steps
To a round bottom flask fitted with a Dean-Stark trap was added a mixture of 19.54 g (116 mmol) of 4-fluoro-2-methoxyacetophenone, 15.29 mL (174 mmol) of methyl cyanoacetate, 1.42 mL (13 mmol) of benzylamine, and 6.6 mL of acetic acid in 170 mL of toluene and the mixture was warmed at reflux. The reaction was monitored by TLC (EtOAc-hexanes, 2:8). After 18 hours, the reaction was then cooled and concentrated in vacuo to afford a dark, orange oil. The crude oil was distilled (Kugelrohr) at 130° C. under vacuum to remove unreacted 4-fluoro-2-methoxyactophenone. The crude was then passed through a pad of silica gel using a 10% EtOAc in a 1:1 mixture of dichloromethane in hexanes to afford 27.64 g (95%) of 2-cyano-3-(4-fluoro-2-methoxyphenyl)but-2-enoic acid methyl ester as a light orange oil which was a mixture of geometric isomers.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07268152B2 |
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| Source dataset | uspto-grants-2007_09 |
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| ORD ID | ord-7021e79579874f33a3e744b972c2a6d2 |
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| Source note | uspto-grants-2007_09 |
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