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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2217129Generated: November 1, 2026

Water → HCID 159518958, compound

https://huagongshe.com/reaction/2217129

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBromineHCID 24408—
Reactant10H-PhenoselenazineHCID 3083559—
ReactantHCID 159425053HCID 159425053—
SolventAcetic AcidHCID 176—
ProductHCID 159518958HCID 15951895817%

Reaction Steps

To a stirred solution of phenoselenazine (1.00 g) in glacial acetic acid (170 cm3), under nitrogen and cooled in an ice-bath was added a solution of bromine (10 cm3) in glacial acetic acid (10 cm3). After 10 minutes the reaction mixture was poured into rapidly stirred water (400 cm3). The resultant 3,7-dibromo-phenoselenazin-5-ylium bromide was deposited as a dark solid and was collected by filtration, washed with diethyl ether and dried. A portion of the product (1.24 g) was added to a vigorously stirred solution of dibutylamine (5.00 g) in dichloromethane (200 cm3) under an atmosphere of nitrogen. The reaction mixture was stirred for 18 hours and then washed successively with water, dilute aqueous hydrobromic acid (5% w/w) and finally water. The organic phase was dried (MgSO4) and the solvent removed by rotary evaporation. Flash column chromatography over silica gel 60 A was performed on the crude material using a mobile phase of chloroform with increasing methanol content to a maximum of 2%. 3,7-Bis-(N,N-dibutylamino)-phenoselenazin-5-ylium bromide was isolated as a dark blue solid in 17% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07407948B2
Source datasetuspto-grants-2008_08
ORD IDord-2c8b78486dca44619b6ddeb0c0a57e06
Source noteuspto-grants-2008_08