HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1075721Generated: October 30, 2026
Water → 4-Methyl-3-nitro-1,1,1-trifluoro-2-pentanol
https://huagongshe.com/reaction/1075721
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,2,2-Trifluoro-1,1-ethanediol | HCID 67901 | — |
| Reactant | 2-Methyl-1-nitropropane | HCID 69367 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | 4-Methyl-3-nitro-1,1,1-trifluoro-2-pentanol | HCID 18792076 | 84% |
Reaction Steps
3A Molecular sieves (27.04 g) were heated at 120° C. under vacuum for 20 hours and added to a solution of 2-methyl-1-nitropropane (13.0 g) in methyl tert-butyl ether (420 ml). The mixture was stirred for 5 minutes, potassium carbonate (64.5 g) added and the mixture stirred a further 30 minutes. The mixture was cooled to 15° C. and fluoral hydrate (22.0 g) was added over 30 minutes. The reaction mixture was stirred at ambient temperature for 16 hours, then cooled to 15° C. and water (270 ml) added. After stirring for 5 minutes at ambient temperature, the organic phase was separated and washed with 10% aqueous potassium carbonate, 2M hydrochloric acid solution and water. Solvent was then removed by evaporation under reduced pressure at a temperature below 40° C. and the oil azeotroped dry with isopropyl alcohol at a temperature below 50° C. to give 4-methyl-3-nitro-1,1,1-trifluoro-2-pentanol (21.3 g) as an oil which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05907043 |
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| Source dataset | uspto-grants-1999_05 |
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| ORD ID | ord-7867d9f360f84881b503d647945cbcc6 |
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| Source note | uspto-grants-1999_05 |
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