Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 68510015 | HCID 68510015 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 57808084 | HCID 57808084 | 100% |
Reaction Steps
To a solution of (E)-methyl 3-(2-methyl-6-(trifluoromethyl)pyridin-3-yl)acrylate (Gray, M.; Andrews, I. P.; Hook, D. F.; Kitteringham, J.; Voyle, M. Tet. Lett. 2001, 41, 6237-6240.) (150 mg, 0.61 mmol) in MeOH (2.0 mL) was added 1M NaOH (aq.) (1.8 mL). The reaction mixture was stirred for 2 h at 40° C. The volatiles were then evaporated and the remaining water phase neutralized with 1M HCl (aq). The title compound (141 mg, 0.61 mmol, quant.), which precipitated as a white solid, was filtered off and dried under vacuum at 45° C. This material was used directly in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08318768B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-9779d21b08e64c498eeb649296d3790b |
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| Source note | uspto-grants-2012_11 |
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