HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxalyl chloride → HCID 10376503, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 11745511 | HCID 11745511 | — |
| Product | HCID 10376503 | HCID 10376503 | — |
| Product | HCID 11097378 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05241116 |
| Source dataset | uspto-grants-1993_08 |
| ORD ID | ord-fc18d970f20346379416e939880d46c3 |
| Source note | uspto-grants-1993_08 |