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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl 3-(trimethylsilyl)propynoate | HCID 568601 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | Methyl 3-[(6-chloropyridazin-3-yl)methyl]-4-methoxybenzoate | HCID 57531225 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 3-[1-(6-chloropyridazin-3-yl)-2-oxo-4-(trimethylsilyl)but-3-yn-1-yl]-4-methoxybenzoate | HCID 57531244 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07482345B2 |
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| Source dataset | uspto-grants-2009_01 |
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| ORD ID | ord-0da6cc5dba5a4bcbbc4969e7a8ac72c1 |
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| Source note | uspto-grants-2009_01 |
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