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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1516231Generated: November 3, 2026

Boron tribromide → HCID 57417096, compound

https://huagongshe.com/reaction/1516231

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
Reactant4-Bromo-2-(2-(4-methoxyphenyl)propan-2-yl)pyridineHCID 57417097—
SolventDichloromethaneHCID 6344—
ProductHCID 57417096HCID 57417096—

Reaction Conditions

Temperature0 °C

Reaction Steps

BBr3 (1M in DCM, 23 mmol, 8 eq) is added dropwise to a cold (0° C.) solution of 4-bromo-2-[1-(4-methoxy-phenyl)-1-methyl-ethyl]-pyridine (Step 31.3) (0.878 g, 2.87 mmol) in DCM (42 mL), under an argon atmosphere. The reaction mixture is stirred for 1 h at 0° C., allowed to warm to rt, stirred for 18 h, cooled to 0° C. and quenched by addition of anhydrous MeOH. The mixture is concentrated, diluted with a 6M aqueous solution of HCl, stirred for 1 h, neutralized to pH 7 and extracted with DCM. The organic phase is dried (Na2SO4), filtered and concentrated. The residue is used without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08227462B2
Source datasetuspto-grants-2012_07
ORD IDord-8154d020a5cc40b1b593f21ebfeeccf0
Source noteuspto-grants-2012_07