HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 264824Generated: October 25, 2026
Toluene → ethyl 2,2-bisfluoromethyl-6-trifluoromethyl-2H-1-benzopyran-4-carboxylate
https://huagongshe.com/reaction/264824
Participants
| Role | Name | HCID | Charge |
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| Reactant | Toluene | HCID 1140 | — |
| Reactant | ethyl 2,2-bisfluoromethyl-6-iodo-2H-1-benzopyran-4-carboxylate | HCID 19037016 | — |
| Reactant | Potassium trifluoroacetate | HCID 23662811 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | ethyl 2,2-bisfluoromethyl-6-trifluoromethyl-2H-1-benzopyran-4-carboxylate | HCID 19037095 | 59.8% |
Reaction Steps
A mixture of 1.00 g of ethyl 2,2-bisfluoromethyl-6-iodo-2H-1-benzopyran-4-carboxylate, 0.84 g of potassium trifluoroacetate, 1.18 g of cuprous iodide, 4 ml of toluene and 10 ml of N,N-dimethylformamide was heated with stirring at 150° C. for 5.5 hours in a nitrogen gas atmosphere while removing toluene. The reaction mixture was added to a mixed solution of 2N hydrochloric acid and ethyl acetate, and an insoluble material was separated by filtration using celite. The organic layer was separated from the filtrate, and the aqueous layer was extracted with ethyl acetate. The resulting organic layers were combined, washed with a brine, dried over sodium sulfate and concentrated under reduced pressure. The resulting residue was subjected to silica gel column chromatography (an eluting solvent, ethyl acetate:hexane =10:1) to obtain 0.51 g of ethyl 2,2-bisfluoromethyl-6-trifluoromethyl-2H-1-benzopyran-4-carboxylate as an oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05646310 |
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| Source dataset | uspto-grants-1997_07 |
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| ORD ID | ord-2e1e4b4c1fbe43408df122cb91c8598a |
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| Source note | uspto-grants-1997_07 |
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