HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1486441Generated: October 30, 2026
Water → Hexanoic acid, 5-oxo-, 1,1-dimethylethyl ester
https://huagongshe.com/reaction/1486441
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | tert-Butyl acetate | HCID 10908 | — |
| Reactant | 4-Acetylbutyric acid | HCID 18407 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Catalyst | Perchloric Acid | HCID 24247 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Hexanoic acid, 5-oxo-, 1,1-dimethylethyl ester | HCID 11008632 | 85% |
Reaction Steps
To a solution of 5-oxohexanoic acid (25 g, 192 mmol) in t-butyl acetate (600 mL) was added perchloric acid (500 μL, 8.31 mmol) and the resulting pale yellow solution was allowed to stir at room temp, with a drying tube in place, for 65 h. The reaction was diluted with ethyl acetate (400 mL) and then quenched with a mixture of sodium bicarbonate (50 g, 595 mmol) and water (100 mL). The organic layer was extracted with saturated aqueous sodium bicarbonate (5×150 mL), water (1×100 mL), brine (1×75 mL), dried over sodium sulfate, and filtered. The solvent was removed in vacuo to give the title compound (30.55 g, 85%) as a light oil. 1H NMR (500 MHz, chloroform-d) δ 2.50 (t, J=7.2 Hz, 2H), 2.25 (t, J=7.3 Hz, 2H), 2.16 (s, 3H), 1.89-1.83 (m, 2H), 1.46 (s, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09427442B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-97419ed876804c7b85937fbe14b541af |
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| Source note | uspto-grants-2016_08 |
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