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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207060Generated: November 2, 2026

Ethyl Acetoacetate → HCID 117992591, compound

https://huagongshe.com/reaction/2207060

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetoacetateHCID 8868—
ReactantSodium hydrideHCID 24758—
ReactantMethyl 4-(bromomethyl)-3-methoxybenzoateHCID 2759828—
SolventTetrahydrofuranHCID 8028—
ProductHCID 117992591HCID 117992591—

Reaction Conditions

Temperature70 °C

Reaction Steps

NaH (60% in mineral oil, 1.5 g) was added portion-wise over 10 mins to a solution of ethyl acetoacetate (4.4 mL) in THF (60 mL) at 0° C. The mixture was then stirred for 10 mins. Then, a solution of methyl 4-(bromomethyl)-3-methoxybenzoate (7.5 g) in THF (40 mL) was added and the mixture was warmed to 70° C. and stirred for 15 h. The mixture was then poured into ice/water (300 mL) and stirred for 30 mins. The resulting aqueous mixture was extracted with EtOAc. The organic extracts were combined, dried and concentrated in vacuo to provide crude product. The reaction was repeated on the same scale. The two batches of crude product were combined and purified by flash column chromatography on silica gel to give the sub-title compound (15 g) as a colourless oil; 1H NMR (300 MHz, CDCl3) δ=7.48 (1H, dd), 7.45 (1H, d), 7.24 (1H, d), 4.05 (2H, q), 3.95 (1H, dd), 3.86 (3H, s), 3.84 (3H, s), 3.10 (1H, dd), 3.00 (1H, dd), 2.17 (3H, s), 1.09 (3H, t).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376398B2
Source datasetuspto-grants-2016_06
ORD IDord-156a6ede34404a9d8588b566c852f069
Source noteuspto-grants-2016_06