Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1778265Generated: November 1, 2026

Methyl 4,8-dibromoquinoline-6-carboxylate → Bis(4-chlorophenyl)(4,8-dibromoquinolin-6-yl)methanol

https://huagongshe.com/reaction/1778265

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4,8-dibromoquinoline-6-carboxylateHCID 118324078—
ReactantHCID 178478191HCID 178478191—
SolventTetrahydrofuranHCID 8028—
ProductBis(4-chlorophenyl)(4,8-dibromoquinolin-6-yl)methanolHCID 118324099—

Reaction Steps

A solution of (4-chlorophenyl)magnesium bromide (2.02 mL, 1.0 M in THF) was dropwise added to a suspension of methyl 4,8-dibromoquinoline-6-carboxylate (0.2 g, 0.58 mmol) in THF (5 mL) at room temperature. The resulting mixture was slowly dissolved and became a clear solution after 30 min. During this period of time, cooling was needed, when the temperature of the reaction mixture rose above room temperature. After 2 hr, the reaction was quenched with ice water and saturated NH4Cl followed by EtOAc. The aqueous layer was extracted with EtOAc. The combined organics were concentrated and purified by silica column (25-30% EtOAc/hexanes) chromatography to yield bis(4-chlorophenyl)(4,8-dibromoquinolin-6-yl)methanol. (M+H)+: 536, 540, 541

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09266835B2
Source datasetuspto-grants-2016_02
ORD IDord-d2ecffc3a3c544d0999760b4fd0e15bb
Source noteuspto-grants-2016_02