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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 560949Generated: October 26, 2026

Dibromonaphthalic anhydride → Naphthalic anhydride

https://huagongshe.com/reaction/560949

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDibromonaphthalic anhydrideHCID 87118624—
SolventDiethyl EtherHCID 3283—
ProductNaphthalic anhydrideHCID 6693—

Reaction Steps

The following morning thin-layer chromatography showed only a trace presence of the dibromonaphthalic anhydride. The reaction mixture was cooled to room temperature followed by the addition of 350 ml of ether. The. triethylamine hydrobromide byproduct was removed by filtration. The filtrate was concentrated on the rotary evaporator, to give the diphenylethynyl derivative of the 1,8-naphthalic anhydride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063168B2
Source datasetuspto-grants-2011_11
ORD IDord-ee79eb69617e456a8906bb8d02ec4325
Source noteuspto-grants-2011_11