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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1757510Generated: October 25, 2026

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

https://huagongshe.com/reaction/1757510

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Methoxy-N-methylbenzamideHCID 569575—
Reactant3-(4-(Dimethylamino)benzyloxy)phenylacetyleneHCID 19388226—
ReactantLithium bis(trimethylsilyl)amideHCID 57426343—
SolventTetrahydrofuranHCID 8028—
Product1-Phenyl-3-[3-(4-(dimethylamino)benzyloxy)phenyl]-2-propyne-1-oneHCID 19388218—

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-(dimethylamino)benzyloxy)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. Alternatively, compounds of formula (1) can be prepared according to the procedure set forth in Scheme B, wherein all substituents, unless otherwise indicated, are previously described. ##STR3##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05446068
Source datasetuspto-grants-1995_08
ORD IDord-811a5c27251840fcad575856719bd0b2
Source noteuspto-grants-1995_08