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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 133215Generated: October 25, 2026

Methyl iodide → 1-Methyl-4-phenyl-3,4-dihydrocarbostyril

https://huagongshe.com/reaction/133215

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant4-Phenyl-3,4-dihydroquinolin-2(1h)-oneHCID 272509—
SolventTetrahydrofuranHCID 8028—
Product1-Methyl-4-phenyl-3,4-dihydrocarbostyrilHCID 12101548—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of NaH (1.2 eq., 0.537 g of 60% dispersion in mineral oil) in THF (50 mL) under N2 at 0° C. was added the product from Step A (1.0 eq., 2.50 g) in THF (50 mL) via cannula over a period of 5 minutes. The resulting pale yellow mixture was stirred at 0° C. for 10 minutes, then MeI (2.0 eq., 1.39 mL) was added. The opaque yellow mixture was allowed to slowly (ice bath not removed) warm to ambient temperature with stirring for 15 hours. 1M Aq. HCl (50 mL) and EtOAc (250 mL) were added and the phases partitioned. The organic phase was washed with dilute NaHCO3 (1×100 mL), brine (1×100 mL), then dried over MgSO4, filtered, concentrated, and the residue purified by flash chromatography eluting with CH2Cl2/EtOAc (19:1 gradient to 15:1) to provide 1-methyl-4-phenyl-3,4-dihydrocarbostyril.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07390801B2
Source datasetuspto-grants-2008_06
ORD IDord-f6e2c41567204da4b4c5ac3b00df0aa8
Source noteuspto-grants-2008_06