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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2396066Generated: October 30, 2026

Boron tribromide → HCID 22918394, compound

https://huagongshe.com/reaction/2396066

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantHCID 22918430HCID 22918430—
SolventDichloromethaneHCID 6344—
ProductHCID 22918394HCID 22918394—

Reaction Steps

To a solution of 219 mg (0.56 mmol) of 4-anilino-5-(3,4-dimethoxy-anilino)-phthalimide in 5 ml of dichloromethane, a solution of 270 μl (2.8 mmol) boron tribromide in 3 ml of dichloromethane is added dropwise at RT. The reaction mixture is stirred for 5 hours at RT and then quenched with 5 ml of water, and the phases are separated. The water phase is extracted three times with ethyl acetate. The organic phases are combined and washed twice with water, dried over magnesium sulfate and concentrated by evaporation. Excluding light, the evaporation residue is chromatographed with ethylacetate/hexane2:1 on a silica gel column (precoated with 0.1 g of sodium ascorbate per g silica gel) that is cooled with ice-water (double jacket), and the productfractions are combined and concentrated by evaporation. Recrystallization from ethyl acetate/dichloromethane/hexane yields the title compound in theform of orange crystals, FAB-MS: 362 [M+ +H].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05491144
Source datasetuspto-grants-1996_02
ORD IDord-c6bedd6f6ca14d54bb83bc49114e8f4e
Source noteuspto-grants-1996_02