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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1706843Generated: October 31, 2026

Bromide ion → HCID 23337263, compound

https://huagongshe.com/reaction/1706843

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromide ionHCID 259—
ReactantDiethyl EtherHCID 3283—
ReactantTetrahydrofuranHCID 8028—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 23337251HCID 23337251—
ProductHCID 23337263HCID 23337263—

Reaction Steps

A suspension was prepared from 4.3 g. of 1H-pyrrolo[1,2,3-de]quinoxalin-2,5,6(3H)-trione in 200 ml. of THF. 16 ml. of 2.83 M phentlmagnesium bromide solution in diethyl ether (phenyl Grignard reagent) were added thereto while maintaining the temperature in the range 10°-15° C. The resulting reaction mixture was stirred overnight after which time, 200 ml. of a saturated aqueous amonium chloride solution were added. An additional 1500 ml. of diethylether were added and the ethereal layer decanted from the solids. The ethereal layer was dried and the ether removed therefrom in vacuo. The resulting residue, comprising 6-hydroxy-6-phenyl-1H-pyrrolo[1,2,3-de]quinoxalin-2,5(3H,6H)-dione melted at 259°-62° C. with decomposition after recrystallization from methanol; yield=2.4 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE030314
Source datasetuspto-grants-1980_06
ORD IDord-79563bc1cf8e409d9176788d794fa39d
Source noteuspto-grants-1980_06