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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 36919Generated: October 24, 2026

Methyl acetoacetate → HCID 131719005, compound

https://huagongshe.com/en/reaction/36919

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl acetoacetateHCID 7757—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium hydrideHCID 24758—
Reactant(E)-3-[4-(4-Fluorophenyl)-6-isopropyl-2-methoxy-3-methoxymethyl-pyridin-5-yl]-prop-2-enalHCID 19936689—
ReactantButyllithiumHCID 178418339—
CatalystZincchlorideHCID 3007855—
SolventDiethyl EtherHCID 3283—
SolventHexaneHCID 8058—
SolventAmmonium ChlorideHCID 25517—
ProductHCID 131719005HCID 131719005—

Reaction Steps

0.35 ml (3.3 mmol) of methyl acetoacetate are added dropwise under nitrogen to a suspension of 80 mg (3.4 mmol) of sodium hydride in 3 ml of dry tetrahydrofuran at -5° C. After 15 min, 2.3 ml (3.3 mmol) of 15% strength butyllithium in n-hexane and 3.3 ml (3.3 mmol) of a 1 molar zinc chloride solution in ether are added dropwise at the same temperature and the mixture is stirred for 15 min. 530 mg (1.5 mmol) of the compound from Example 10 dissolved in 8 ml of dry tetrahydrofuran are then added dropwise and the mixture is stirred at -5° C. for 30 min. The reaction solution is cautiously diluted with 100 ml of saturated aqueous ammonium chloride solution and the mixture is extracted three times with 100 ml of ether each time. The combined organic phases are washed twice with saturated sodium hydrogen carbonate solution and once with saturated sodium chloride solution, dried over sodium sulphate and concentrated in vacuo.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05418243
Source datasetuspto-grants-1995_05
ORD IDord-b62755906215485e999eb3fe515012ae
Source noteuspto-grants-1995_05