Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | HCID 59199277 | HCID 59199277 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59199292 | HCID 59199292 | — |
Reaction Steps
N-(2-methoxy-5-(trifluoromethyl)phenyl) pivalamide (1 eq) was azeotrope with toluene (x=3). Dissolved in THF, cooled to −50° C. and added n-BuLi (2 eq, 2.5M solution in hexane) dropwise. The reaction mixture was stirred at −50° C. for 1 h then warmed to −10° C. in 30 min. Stirred at this temperature for 30 min then CO2 gas was passed through cylinder into the reaction mixture at −10 to 0° C. for 1 h. The reaction mixture was warmed to room temperature and stirred overnight. The reaction was poured to water and extracted with ethyl acetate. (EtOAc extracts contained starting material). The aq layer pH was adjusted to 1-2 and product was extracted with ethyl acetate (x=3). The ethyl acetate extracts were combined, washed with brine and dried over sodium sulfate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07932262B2 |
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| Source dataset | uspto-grants-2011_04 |
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| ORD ID | ord-e906e6aa291b4805b58909b644c17008 |
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| Source note | uspto-grants-2011_04 |
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