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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 579467Generated: October 26, 2026

Methanol → Ethyl 4-methoxy-3-oxobutanoate

https://huagongshe.com/reaction/579467

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantDimethylformamideHCID 6228—
ReactantSodium hydrideHCID 24758—
Reactant3-Bromo-7-hydroxy-4-methylchromen-2-oneHCID 5337545—
SolventHydrochloric AcidHCID 313—
ProductEthyl 4-methoxy-3-oxobutanoateHCID 1264509915.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

NaH (7.71 g, 192.7 mmol) was suspended in DMF (110 mL). The solution of MeOH (2.64 g, 82.5 mmol) in DMF (55 mL) was added drop wise at 0° C. After that, the mixture was stirred at 0° C. for 30 min. The solution of compound 1 (9.54 g, 57.9 mmol) in DMF (55 mL) was added dropwise at 0° C., then the reaction mixture was allowed to warm slowly to RT and stirred for 16 h. The reaction mixture was diluted with 1N HCl (400 mL), extracted with MTBE (250 mL×3). The combined organic layer was washed with H2O (200 mL×5), dried over Na2SO4, filtered, concentrated, purified by silica gel column (PE:EA=10:1) afforded ethyl 4-methoxy-3-oxobutanoate (1.4 g, 15.1%) as light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040714B2
Source datasetuspto-grants-2015_05
ORD IDord-9e7544d2fee74e90bb23995b25649632
Source noteuspto-grants-2015_05