HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 262740Generated: October 26, 2026
Potassium Carbonate → 3,4-Bis(2,2,2-trifluoroethoxy)nitrobenzene
https://huagongshe.com/reaction/262740
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,2,2-Trifluoroethyl trifluoromethanesulfonate | HCID 80366 | — |
| Reactant | 4-Nitrocatechol | HCID 3505109 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 3,4-Bis(2,2,2-trifluoroethoxy)nitrobenzene | HCID 13370433 | — |
Reaction Steps
To a refluxing mixture of 12.7 g. (0.092 mole) of potassium carbonate, 21.3 g. (0.092 mole) of 2,2,2-trifluoroethyl trifluoromethanesulfonate and 62 ml. of acetone is added dropwise 6.2 g. (0.040 mole) of 4-nitrocatechol in 62 ml. of acetone over about 2.5 hours. Refluxing is continued for a total of 24 hours, then the solution is evaporated. The residue is mixed with equal volumes of water and diethyl ether. The ether layer is separated, washed with water and saturated sodium chloride solution and dried. Evaporation provides crude 3,4-bis(2,2,2-trifluoroethoxy)nitrobenzene. Chromatographic purification on a silica gel column is effected by eluting with mixtures of chloroform and hexane. Recrystallization from cyclohexane with a small amount of benzene provides solid product, m.p. 63°-65° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04154941 |
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| Source dataset | uspto-grants-1979_05 |
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| ORD ID | ord-212aba99a9fb43f4bbf7b4c6ede818b9 |
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| Source note | uspto-grants-1979_05 |
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