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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Methoxy-N-methylbenzamideHCID 569575—
Reactant3-(4-Ethoxybenzyloxy)phenylacetyleneHCID 19388221—
ReactantLithium bis(trimethylsilyl)amideHCID 57426343—
SolventTetrahydrofuranHCID 8028—
Product1-Phenyl-3-[3-(4-ethoxybenzyloxy)phenyl]-2-propyne-1-oneHCID 19388229—

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-(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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05446068
Source datasetuspto-grants-1995_08
ORD IDord-937ce94e98ee403e89ed4d1aa1bb21cf
Source noteuspto-grants-1995_08