Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 68514079 | HCID 68514079 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68514159 | HCID 68514159 | 100% |
Reaction Steps
To a solution of cyclohexyl{2-(ethoxymethyl)-5-[4-(trifluoromethyl)phenyl]furan-3-yl}methanol (1.8 g) in tetrahydrofuran (30 mL) were added oxalyl chloride (0.6 mL) and triethylamine (1.0 mL) at 0° C., and the mixture was stirred at 0° C. for 1 hr. The reaction mixture was poured into water, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over magnesium sulfate. The solvent was evaporated under reduced pressure to give the title compound (1.9 g, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08309580B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-5d85850f6bbd44ef82acf79b8043f94a |
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| Source note | uspto-grants-2012_11 |
|---|