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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 382726Generated: October 23, 2026

Methanol → Ethyl 4-methoxy-3-oxobutanoate

https://huagongshe.com/en/reaction/382726

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium IodideHCID 5238—
ReactantSodium hydrideHCID 24758—
ReactantEthyl 4-chloroacetoacetateHCID 69484—
CatalystTetrabutylammonium BromideHCID 74236—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 4-methoxy-3-oxobutanoateHCID 12645099—

Reaction Steps

A mixture of 15.8 g of ethyl 4-chloroacetoacetate (96.2 mmol) and 3.39 g of methanol (106 mmol) in 10 mL of THF were added dropwise to a stirred suspension of 4.62 g of 60% NaH (in mineral oil), 1.60 g of NaI (9.62 mmol), and 3.10 g of tetrabutylammonium bromide (9.62 mmol) in 40 mL of THF at −30° C. over a period of 1.5 hrs. The reaction mixture was then warmed to room temperature and stirred for 4 days. The reaction mixture was cooled to −30° C., quenched with 5 mL of methanol, and warmed to room temperature. The reaction mixture was poured into 0.5 L of 10% HCl solution, extracted with 2×100 mL of EtOAc, dried (Na2SO4), and the solvent was removed in vacuo. The crude product was distilled. The fraction boiling at 65-70° C. (0.3 mm Hg) was collected and used in the next experiments after spectral characterization.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06310076B1
Source datasetuspto-grants-2001_10
ORD IDord-68982d2e2d8742519a83b521712b6342
Source noteuspto-grants-2001_10