HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1435161Generated: October 30, 2026
Ethyl 2-methylacetoacetate → HCID 57937746, compound
https://huagongshe.com/reaction/1435161
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl 2-methylacetoacetate | HCID 701 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-Bromopentyl acetate | HCID 85140 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 57937746 | HCID 57937746 | 49% |
Reaction Steps
In a 1 L three necked flask equipped with a mechanical stirrer and reflux condenser was placed dry toluene (300 ml). The system was flushed with argon and sodium hydride (Aldrich, 60% dispersion in mineral oil) (7.2 g, 1.2 eq.) was added. Ethyl-α-methylacetoacetate (Aldrich, 21 g, 0.15 mole) was added with stirring over a 30 minutes. The resulting solution was heated under reflux for 2 hours and cooled slightly. (Note: Reaction mixture becomes a thick paste and a mechanical stirrer is essential). 5-Bromopentylacetate (Aldrich, 31.5 g, 15 mol) was added (all at once) and the suspension was heated under reflux for 12 hr, cooled, filtered and the solvent evaporated under reduced pressure. The residue was distilled under vacuum to yield 20 g (45%) of colorless liquid, b.p 90-92 (0.5 mm). 1H NMR in CDCl3 δ, 4.1-4.2 (m, 2H, O—CH2CH3): 3.5 (t, J=7 Hz, 2H, CH2OCO—); 2.2 (s, 3H, CH3CO); 2.1 (s, 3H, —COCH3); 1.5-2.0 (m, 10H, 4-(CH2)2, C—CH3, OCH2CH3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07615646B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-36c983e8a166494c97d45b3a29ae14c9 |
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| Source note | uspto-grants-2009_11 |
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