Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosgene | HCID 6371 | — |
| Reactant | HCID 19892243 | HCID 19892243 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 19892242 | HCID 19892242 | 45.2% |
Reaction Steps
A mixture of 0.35 g (1 mmol) of N'-(2,6-dinitro-4-trifluoromethylphenyl)-2,2-dimethylpropionhydrazide, 0.3 g (3.1 mmols) of phosgene and 2.1 ml of toluene was heated to reflux for 2.5 hours (inner temperature of 59° C.). A solution (0.7 ml) of 0.1 g (1 mmol) of phosgene in toluene was further added to the reaction mixture followed by heating to reflux for further 2.5 hours. An excess of phosgene and toluene were distilled off and the residue was taken up in 20 ml of ether. After washing with saturated sodium chloride aqueous solution, the solution was dried over anhydrous sodium sulfate and then concentrated under reduced pressure. The thus obtained crude product was subjected to silica gel column chromatography to give 0.17 g of 5-(1,1-dimethylethyl)-3-(2,6-dinitro-4-trifluoromethylphenyl)-1,3,4-oxadiazolin-2-one.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05124341 |
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| Source dataset | uspto-grants-1992_06 |
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| ORD ID | ord-af552e96280748a1a29f3224409edaae |
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| Source note | uspto-grants-1992_06 |
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