HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 481858Generated: November 2, 2026
Methyl acetoacetate → HCID 54721558, compound
https://huagongshe.com/reaction/481858
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl acetoacetate | HCID 7757 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 1274032 | HCID 1274032 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 54721558 | HCID 54721558 | — |
Reaction Steps
The title compound was prepared as described in General Method 1 using 0.22 mL of methyl acetoacetate, 90 mg of NaH 60% dispersion in oil, 1 mL of 2.1M n-butyl lithium in hexane, 500 mg of 3-(3,4-methylenedioxyphenyl)propiophenone and 15 mL of tetrahydrofuran. After addition of the ketone, the reaction was stirred for 15 minutes at 0° C. then allowed to warm to room temperature and stirred for 2 hours. The crude product was triturated from diethyl ether to afford a solid (m.p. 112°-114° C.). 1H NMR (CDCl3) δ2.20-2.28 (m, 2H), 2.37-2.44 (m, 1H), 2.61-2.69 (m, 1H), 2.95 (dd, 2H), 3.32 (dd, 2H), 5.90 (s, 2H), 6.52-6.70 (m, 3H), 7.33-7.44 (m, 5H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05789440 |
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| Source dataset | uspto-grants-1998_08 |
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| ORD ID | ord-0b6c12c4ef70461bb021f79b1a1cb6b3 |
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| Source note | uspto-grants-1998_08 |
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