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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1453646Generated: October 31, 2026

Sodium hydride → 4-(3-Bromo-5-methoxy-benzyl)-3,4-dihydro-1H-quinoline-2-one

https://huagongshe.com/reaction/1453646

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantHydrocarbostyrilHCID 64796—
Reactant1-Bromo-3-(bromomethyl)-5-methoxybenzeneHCID 12276449—
SolventDimethylformamideHCID 6228—
Product4-(3-Bromo-5-methoxy-benzyl)-3,4-dihydro-1H-quinoline-2-oneHCID 22324259—

Reaction Steps

3,4-Dihydro-2(1H)-quinolinone was purchased from Aldrich Chemical Co. (Cat. No. 41,593-6) and used without purification in this step. 0.45 grams of 3,4-dihydro-2(1H)-quinolinone (3.0 mmole) was dissolved in 15 ml dimethylformamide and cooled in an ice bath. 0.2 grams (4.5 mmole) of sodium hydride (60% wt. in oil ) was added to this solution, and after 5 minutes 0.84 grams 3-bromo-5-methoxy-benzylbromide (3 mmol) was added thereto all at once. The mixture was stirred at ice bath temperature for 1 hour and then quenched by addition of 1% hydrochloric acid. The reaction mix was extracted with ethyl acetate, which was evaporated under reduced pressure to give an oil, which was chromatographed with medium pressure eluting using 10% ethyl acetate in hexanes to yield 0.8 grams of solid 4-(3-bromo-5-methoxy-benzyl)-3,4-dihydro-1H-quinoline-2-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07476675B2
Source datasetuspto-grants-2009_01
ORD IDord-a0bf169bfbea47dbbb490f8183a65566
Source noteuspto-grants-2009_01