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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Methoxy-N-methylbenzamideHCID 569575—
Reactant1-Ethynyl-3-((4-methoxybenzyl)oxy)benzeneHCID 15281122—
ReactantLithium bis(trimethylsilyl)amideHCID 57426343—
SolventTetrahydrofuranHCID 8028—
Product1-Phenyl-3-[3-(4-methoxybenzyloxy)phenyl]-2-propyne-1-oneHCID 9840975—

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05446068
Source datasetuspto-grants-1995_08
ORD IDord-48780852258f42e2936b931423a3798e
Source noteuspto-grants-1995_08