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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6488Generated: October 26, 2026

N-Methoxy-N-methylbenzamide → 1-Phenyl-3-[3-(4-methoxybenzyloxy)phenyl]-2-propyne-1-one

https://huagongshe.com/reaction/6488

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-(4-methoxybenzyloxy)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 and stir 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 (1st crop) and 0.15 g (2nd crop) of the title compound; mp 79°-80° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05248825
Source datasetuspto-grants-1993_09
ORD IDord-d099e8b2015d49a88b10fcd0cbfb9273
Source noteuspto-grants-1993_09