HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 357825Generated: October 31, 2026
Methyl acetoacetate → HCID 54721631, compound
https://huagongshe.com/reaction/357825
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl acetoacetate | HCID 7757 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 13656084 | HCID 13656084 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 54721631 | HCID 54721631 | — |
Reaction Steps
The title compound was prepared as described in General Method 1 using 1.7 mL of methyl acetoacetate, 630 mg of NaH 60% dispersion in oil, 9.85 mL of 1.6M n-butyl lithium in hexane, 4.0 g of 3-(3,4-dichlorophenyl)propiophenone and 150 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 4 hours. The crude product was triturated from diethyl ether to afford a solid (m.p. 145°-147° C.). 1H NMR (CDCl3) δ 2.18-2.35 (m, 2 H), 2.39-2.50 (m, 1 H), 2.68-2.80 (m, 1 H), 2.96 (dd, 2 H), 3.36 (dd, 2 H), 6.90-7.50 (m, 8 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05840751 |
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| Source dataset | uspto-grants-1998_11 |
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| ORD ID | ord-b5e2bce8327049e79d24259195293c77 |
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| Source note | uspto-grants-1998_11 |
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