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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 355496Generated: October 30, 2026

Methyl acetoacetate → HCID 13461920, compound

https://huagongshe.com/reaction/355496

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl acetoacetateHCID 7757—
Reactant1-BromoheptaneHCID 12369—
ReactantSodiumHCID 5360545—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
ProductHCID 13461920HCID 1346192078%

Reaction Steps

Methyl acetoacetate (20.00 g, 172.2 mmol) was treated with sodium methoxide (NaOMe)/MeOH (freshly prepared by dissolving 4.00 g sodium in 200 mL anhydrous MeOH at 0° C.) at room temperature for 20 minutes. n-Heptyl bromide (24.60 mL, 156.6 mmol, 0.9 equiv.) was added and the solution was refluxed for 24 hours. Methanol was evaporated and the residue was treated with 5% hydrogen sulfate (H2SO4) (100 mL) in acetone (200 mL) at room temperature for 2 hours. Acetone was evaporated and the aqueous layer was extracted with ether (400 mL). The ether extract was then quickly washed with 1N NaOH (100 mL×3), water (100 mL×2), and brine (100 mL×1), and dried over MgSO4. Evaporation of the solvents yielded 33.56 g (78%) crude product as an oil. Rf =0.6 (10% ether/petroleum ether). 1H NMR (400 MHz, CDCl3) δ0.88 (3H, t, J=6.7 Hz), 1.20-1.45 (10H, br m), 1.78-1.91 (2H, m), 2.22 (3H, s), 3.42 (1H, t, J=7.4 Hz), 3.73 (3H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05831004
Source datasetuspto-grants-1998_11
ORD IDord-698a7197aa804f2a80cbf3632e3951b7
Source noteuspto-grants-1998_11