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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1435161Generated: October 30, 2026

Ethyl 2-methylacetoacetate → HCID 57937746, compound

https://huagongshe.com/reaction/1435161

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-methylacetoacetateHCID 701—
ReactantSodium hydrideHCID 24758—
Reactant5-Bromopentyl acetateHCID 85140—
SolventTolueneHCID 1140—
ProductHCID 57937746HCID 5793774649%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07615646B2
Source datasetuspto-grants-2009_11
ORD IDord-36c983e8a166494c97d45b3a29ae14c9
Source noteuspto-grants-2009_11