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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2255805Generated: October 30, 2026

Oxalyl chloride → HCID 10376503, compound

https://huagongshe.com/reaction/2255805

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 11745511HCID 11745511—
ProductHCID 10376503HCID 10376503—
ProductHCID 11097378HCID 11097378—

Reaction Steps

A solution of 1,4-dinitrocubane (Eaton, P. E.; et al; J. Org. Chem.; 1984, 49, 185; Eaton, P. E.; Wicks, G. E.; J. Org. Chem.; 1988, 53, 5353) in oxalyl chloride was irradiated under a sunlamp for 12 h at room temperature. After removing oxalyl chloride under reduced pressure, the reaction mixture was hydrolyzed and partioned between ethyl acetate and 5% aqueous NaOH. From the organic phase was isolated 2-chloro-1,4-dinitrocubane, 3, and 2,5-dichloro-1,4-dinitrocubane, 4. After acidification of the alkaline layer with HCl and extraction with ethyl acetate, 2-carboxy-1,4-dinitrocubane, 5, was obtained in 68% yield. ##STR1##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05241116
Source datasetuspto-grants-1993_08
ORD IDord-fc18d970f20346379416e939880d46c3
Source noteuspto-grants-1993_08