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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2163328Generated: October 31, 2026

Tetrahydrofuran → HCID 23337263, compound

https://huagongshe.com/reaction/2163328

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 23337251HCID 23337251—
ReactantHCID 178418255HCID 178418255—
SolventDiethyl EtherHCID 3283—
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 a 2.83 M phenylmagnesium 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; yielded = 2.4 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04133884
Source datasetuspto-grants-1979_01
ORD IDord-b94cabd130e940ebb9ecc29d88e5234b
Source noteuspto-grants-1979_01