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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 366957Generated: October 26, 2026

Methyl acetoacetate → Methyl 3-oxo-5-(phenylthio)pentanoate

https://huagongshe.com/reaction/366957

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl acetoacetateHCID 7757—
ReactantSodium hydrideHCID 24758—
Reactant2-Chlorophenyl methyl sulfideHCID 2737363—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Solventtetrahydrofuran HMPAHCID 86583969—
ProductMethyl 3-oxo-5-(phenylthio)pentanoateHCID 1276477222.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of NaH (60%) (815 mg, 20.39 mmol) in THF-HMPA (20 ml, 5 ml) was added methylacetoacetate (2.0 g, 18.5 mmol) in THF (5 ml) at 0° C. The mixture was stirred for 10 min. at 0° C. under nitrogen atmosphere. BuLi (12.3 ml, 20.39 mmol) was dropwise added and the red mixture was stirred for 15 min. at 0° C. Then a solution of chlorothioanisole (2.7 ml, 20.39 mmol) in THF (5 ml) was added to the mixture at 0° C. The mixture was stirred for 1 h at -5° C. The mixture was quenched with H2O, then extracted with AcOEt (100 ml×2). AcOEt layer was washed with H2O (10 ml×2) and brine (10 ml), then dried over MgSO4 and evaporated. The residue was purified by a silica gel column chromatography (150 g, hexane :AcOEt=6:1) to give a colorless oil (1.0 g, 22.7%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06131226
Source datasetuspto-grants-2000_10
ORD IDord-0662be53814b40eda18d24f9bf08d60d
Source noteuspto-grants-2000_10