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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1191331Generated: November 2, 2026

Potassium tert-butoxide → 4-(3-bromophenyl)-6,7-dimethoxy-3-(thiophen-2-yl)quinolin-2(1H)-one

https://huagongshe.com/reaction/1191331

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium tert-butoxideHCID 23665647—
ReactantN-{2-[(3-bromophenyl)carbonyl]-4,5-dimethoxyphenyl}-2-(thiophen-2-yl)acetamideHCID 66849274—
SolventTetrahydrofuranHCID 8028—
Product4-(3-bromophenyl)-6,7-dimethoxy-3-(thiophen-2-yl)quinolin-2(1H)-oneHCID 66899801—

Reaction Steps

To a solution of N-{2-[(3-bromophenyl)carbonyl]-4,5-dimethoxyphenyl}-2-(thiophen-2-yl)acetamide (8 g, 17.4 mmol) in dry THF (80 mL) was added t-BuOK (6 g 52.1 mmol) in portions at 0° C. The reaction mixture was stirred for 1 hour and concentrated under reduced pressure. The residue was diluted with EtOAc (50 mL). The combined organic layers were dried over anhydrous MgSO4, filtered and concentrated in vacuum to afford 4-(3-bromophenyl)-6,7-dimethoxy-3-(thiophen-2-yl)quinolin-2(1H)-one. MS (M+H)=442 and 444.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680116B2
Source datasetuspto-grants-2014_03
ORD IDord-b1b5bf7b116f43a48ff1c5f680d4bf30
Source noteuspto-grants-2014_03