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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1454955Generated: October 30, 2026

Ethyl 3-(trimethylsilyl)propynoate → Methyl 3-[1-(6-chloropyridazin-3-yl)-2-oxo-4-(trimethylsilyl)but-3-yn-1-yl]-4-methoxybenzoate

https://huagongshe.com/reaction/1454955

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3-(trimethylsilyl)propynoateHCID 568601—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantMethyl 3-[(6-chloropyridazin-3-yl)methyl]-4-methoxybenzoateHCID 57531225—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 3-[1-(6-chloropyridazin-3-yl)-2-oxo-4-(trimethylsilyl)but-3-yn-1-yl]-4-methoxybenzoateHCID 57531244—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of methyl 3-[(6-chloropyridazin-3-yl)methyl]-4-methoxybenzoate (10.03 g, 34.2 mmol) in THF (400 mL) was added LHMDS (100 mL, 1M solution in THF) and ethyl 3-(trimethylsilyl)propynoate (6.66 mL, 35.5 mmol) at −78° C. The reaction was warmed to 0° C. and stirred for 0.5 hr until the reaction was complete by LCMS analysis. The reaction was quenched with aqueous NH4Cl and extracted with ethyl acetate. The combined organic layers were washed with 0.5 N HCl, brine, dried over MgSO4, and condensed in vacuo to yield an oil. The crude material was purified via silica gel chromatography (CH2Cl2) to yield the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07482345B2
Source datasetuspto-grants-2009_01
ORD IDord-0da6cc5dba5a4bcbbc4969e7a8ac72c1
Source noteuspto-grants-2009_01