HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1265277Generated: October 31, 2026
Ethyl Acetoacetate → Ethyl 2-acetyl-5,5-dimethyl-4-oxohexanoate
https://huagongshe.com/reaction/1265277
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetoacetate | HCID 8868 | — |
| Reactant | Bromopinacolone | HCID 21642 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Ethyl 2-acetyl-5,5-dimethyl-4-oxohexanoate | HCID 11775940 | 87.4% |
Reaction Steps
Ethyl acetoacetate (1 g, 7.68 mmol) was added dropwise to a suspension of NaH (60% in mineral oil, 338 mg, 8.45 mmol) in toluene (20 mL). The resulting suspension was stirred at rt for 10 min, then treated with 1-bromopinacolone (1.3 g, 7.32 mmol). The mixture was immersed in a 75° C. oil bath, and stirred under Ar for 1 h. The reaction was cooled to rt, diluted with toluene and washed with H2O (2×50 mL). The organic layer was dried over Na2SO4, filtered and concentrated in vacuo to afford crude ethyl 2-acetyl-5,5-dimethyl-4-oxo-hexanoate (1.46 g) which was not purified: 1H NMR (CDCl3, chemical shifts in ppm relative to TMS): 1.166 (s, 9H), 1.277 (t, 3H, J=7.1 Hz), 2.368 (s, 3H), 3.000 (dd, 1H, J=5.8 Hz, J=18.4 Hz), 3.231 (dd, 1H, J=8.2 Hz, J=18.4 Hz), 4.010 (dd, 1H, J=5.8 Hz, J=8.2 Hz), 4.191 (q, 2H, J=7.1 Hz); Field Desorption Mass Spectrometry: m/z 229 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06545108B1 |
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| Source dataset | uspto-grants-2003_04 |
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| ORD ID | ord-036475c5562e46198db830d7bc527952 |
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| Source note | uspto-grants-2003_04 |
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