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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 371706Generated: October 30, 2026

Tetrahydrofuran → HCID 23337263, compound

https://huagongshe.com/reaction/371706

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°-262° C. with decomposition after recrystallization from methanol; yield = 2.4 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04087527
Source datasetuspto-grants-1978_05
ORD IDord-d073e9b7625c458eb01dfae7b9cc4d41
Source noteuspto-grants-1978_05