HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1618086Generated: November 2, 2026
Sulfuric Acid → Butanoic acid, 4,4-difluoro-3-oxo-, ethyl ester
https://huagongshe.com/reaction/1618086
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2,2-Difluoroethylacetate | HCID 137074 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Butanoic acid, 4,4-difluoro-3-oxo-, ethyl ester | HCID 67697 | — |
Reaction Steps
Under nitrogen, 46.7 g (1.168 mol) of sodium hydride (60% dispersion in paraffin) were added to 600 ml of tetrahydrofuran. At 35° C. a mixture of 125 g (1.008 mol) of difluoroethyl acetate and 88.7 g (1.010 mol) of ethyl acetate was added dropwise while the temperature was maintained at below 40° C. This was followed by further stirring at room temperature overnight. The reaction mixture was carefully poured into 1.7 L of ice-water and adjusted to pH 3 with sulphuric acid. The reaction mixture was extracted twice with 500 ml of methyl tert-butyl ether each time, the combined organic phases were washed twice with saturated sodium chloride solution, dried over sodium sulphate and concentrated at 40° C. and 150 mbar before distillation at 60 mbar (Vigreux column). The product was obtained at 85-87° C. as a colourless liquid (104 g, 62% of theory having a purity of >99% (GC)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08765971B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-bbdb639f8dff418295bb231d66c315d8 |
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| Source note | uspto-grants-2014_07 |
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