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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1778293Generated: October 30, 2026

HCID 118324051, compound → HCID 118324147, compound

https://huagongshe.com/reaction/1778293

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 118324051HCID 118324051—
ReactantHCID 178478191HCID 178478191—
SolventTetrahydrofuranHCID 8028—
ProductHCID 118324147HCID 118324147—

Reaction Steps

To a solution of (4-bromoquinolin-6-yl)(4-chlorophenyl)methanone (0.25 g, 0.72 mmol) in THF (5 mL) was slowly added (4-chlorophenyl)magnesium bromide (1.08 mL, 1 M in THF) at 0° C. under the argon. The resulting solution was kept at 0° C. for 3 hr. The reaction was quenched with saturated NH4Cl at 0° C. and the aqueous mixture was extracted with EtOAc 2 times. The combined organics were concentrated and purified by silica column chromatography (20-30% EtOAc/hexanes) to yield (4-bromoquinolin-6-yl)bis(4-chlorophenyl)methanol. (M+H)+: 458, 460.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09266835B2
Source datasetuspto-grants-2016_02
ORD IDord-2aa17aa9303c4a2baa2563b7c393ea33
Source noteuspto-grants-2016_02