HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1757507Generated: October 26, 2026
N-Methoxy-N-methylbenzamide → 1-Phenyl-3-[3-(4-ethoxybenzyloxy)phenyl]-2-propyne-1-one
https://huagongshe.com/reaction/1757507
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Methoxy-N-methylbenzamide | HCID 569575 | — |
| Reactant | 3-(4-Ethoxybenzyloxy)phenylacetylene | HCID 19388221 | — |
| Reactant | Lithium bis(trimethylsilyl)amide | HCID 57426343 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Phenyl-3-[3-(4-ethoxybenzyloxy)phenyl]-2-propyne-1-one | HCID 19388229 | — |
Reaction Steps
Place lithium hexamethyldisilazane (2 mL of a 1M solution in tetrahydrofuran, 2 mmol) and tetrahydrofuran (8 mL) under an argon atmosphere and cool to 0° C. Add a solution of 3-(4ethoxybenzyloxy)phenylacetylene (0.51 g, 2 mmol) in tetrahydrofuran and stir the solution for 45 minutes at 0° C. Add N-methoxy-N-methylbenzamide (0.4 g, 2.4 mmol), remove the cooling bath andstir at room temperature for 1 hour. Partition the mixture between ethyl ether and water, separate the organic phase and dry (MgSO4). Filter and evaporate the solvent in vacuo to yield an oil. Filter through silica gel and elute with 10% ethyl acetate/hexane to yield a crude solid. Purifyby silica gel chromatography to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05446068 |
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| Source dataset | uspto-grants-1995_08 |
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| ORD ID | ord-937ce94e98ee403e89ed4d1aa1bb21cf |
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| Source note | uspto-grants-1995_08 |
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