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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 249564Generated: October 30, 2026

Oxalyl chloride → HCID 10376503, compound

https://huagongshe.com/reaction/249564

Reaction equation

Participants

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

Reaction Steps

A mixture of 1,4-dinitrocubane, 1,(388 mg. 2.0 mmol) in oxalyl chloride (50 mL) was photolyzed under a sunlamp for 18 h at room temperature. Oxalyl chloride was removed on a rotary evaporator and the solid residue was partioned between EtOAc (40 mL) and NaOH solution (5%, 30 mL). After stirring for 3 h, the organic phase was separated, washed with brine, dried over anhydrous Na2SO4 and concentrated under reduced pressure. The residue was chromatographed on silica gel using hexane/CH2Cl2 (1:1) to give 2-chloro-1,4-dinitrocubane 3, m.p. 145°-147° C.; 1H NMR(CDCl3); δ4.84(m, 2H); 4.71 (m, 3H); and 2,5-dichloro-1,4-dinitrocubane, 4, m.p. 188°-190° C.; 1H NMR (CDCl3);δ4.90(dd, 2H); 4.78 (dd,2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05214221
Source datasetuspto-grants-1993_05
ORD IDord-1af9f84a73a845b5be78e771d035ed62
Source noteuspto-grants-1993_05