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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1681263Generated: November 2, 2026

Methyl acetoacetate → HCID 17821749, compound

https://huagongshe.com/reaction/1681263

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl acetoacetateHCID 7757—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 86746403HCID 86746403—
ReactantButyllithiumHCID 178418339—
CatalystZinc bromideHCID 10421208—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 17821749HCID 17821749—

Reaction Steps

0.5 ml (4.5 mmol) of methyl acetoacetate are added dropwise at 0° C.-5° C. under argon to a suspension of 0.15 g (5 mmol) of 80% pure sodium hydride in 6.5 ml of tetrahydrofuran p.a. After 15 minutes in each case, 3.65 ml (6 mmol) of 15% strength butyllithium in hexane are first added dropwise at 0° C. during the course of 10 minutes then a solution of 1.01 g (4.5 mmol) of dry zinc bromide in 4.5 ml of tetrahydrofuran and finally 0.51 g (1.5 mmol) of the compound from Example 123. The mixture is stirred overnight at room temperature, saturated ammonium chloride solution is added slowly, the aqueous phase is extracted using ethyl acetate, and the combined organic phases are washed using saturated sodium chloride solution, dried over sodium sulphate and concentrated. After column chromatography (φ3 cm) on 20 g of silica gel (230-400 mesh) using petroleum ether-ethyl acetate (1:1), 0.17 g (25% of theory) of yellowish oil is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05169857
Source datasetuspto-grants-1992_12
ORD IDord-35bc1a738d24451c87ef678cec627a6d
Source noteuspto-grants-1992_12