HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1757501Generated: October 23, 2026
N-Methoxy-N-methylbenzamide → 1-Phenyl-3-[3-(4-methoxybenzyloxy)phenyl]-2-propyne-1-one
https://huagongshe.com/en/reaction/1757501
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-Methoxy-N-methylbenzamide | HCID 569575 | — |
| Reactant | 1-Ethynyl-3-((4-methoxybenzyl)oxy)benzene | HCID 15281122 | — |
| Reactant | Lithium bis(trimethylsilyl)amide | HCID 57426343 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Phenyl-3-[3-(4-methoxybenzyloxy)phenyl]-2-propyne-1-one | HCID 9840975 | — |
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-(4methoxybenzyloxy)phenylacetylene (0.48 g, 2 mmol) in tetrahydrofuran and stir the brown 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. Recrystallize (hexane, ethyl ether) to yield 0.26 g (lst crop) and 0.15 g (2nd crop) of the title compound; mp 79°-80 C.
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-48780852258f42e2936b931423a3798e |
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| Source note | uspto-grants-1995_08 |
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