Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 12274790 | HCID 12274790 | — |
| Reactant | 4-bromo-2,2-bis(fluoromethyl)-6-trifluoromethyl-2H-1-benzopyran | HCID 18424409 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | HCID 18424422 | HCID 18424422 | 52% |
Reaction Steps
An amount (58 mg) of 4-bromo-2,2-bis(fluoromethyl)-6-trifluoromethyl-2H-1-benzopyran was dissolved in t-butyl methyl ether (2 ml); to the solution, 1.69 M n-butyllithium (0.108 ml) was added at −70° C. under a nitrogen atmosphere and the mixture was stirred for 15 minutes. Then, diethyl thiocarbonate (67 mg) was added dropwise to the reaction mixture, which was stirred for 30 minutes at −70° C. To the reaction mixture, a saturated aqueous solution of ammonium chloride was added, followed by extraction with hexane/ethyl acetate (3/1). The resulting organic layers were washed with a saturated aqueous solution of sodium chloride, dried with anhydrous sodium sulfate and concentrated under reduced pressure; the resulting residue was subjected to silica gel column chromatography (eluent; hexane/ethyl acetate=2/1) to give the titled compound (31 mg) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06455708B1 |
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| Source dataset | uspto-grants-2002_09 |
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| ORD ID | ord-58043ad9375f4a1fadb5552919546b31 |
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| Source note | uspto-grants-2002_09 |
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