HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2295905Generated: October 27, 2026
Dichloromethane → 1-(Ethenyloxy)-2,2-dinitropropane
https://huagongshe.com/reaction/2295905
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Vinyl ether | HCID 8024 | — |
| Reactant | 2,2-Dinitropropanol | HCID 70194 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 1-(Ethenyloxy)-2,2-dinitropropane | HCID 12385928 | 58.8% |
Reaction Steps
A 50 ml single necked, round bottom flask was charged with 20 ml methylene chloride, 0.50 g (7.14 mmole) divinyl ether, 1.07 g (7.14 mmole) 2,2-dinitropropanol (VIII), and 0.1 g red mercuric oxide. The solution was stirred, using a Teflon coated magnetic bar while 100 μl trifluoroacetic acid was added. The reaction flask was then fitted with a water cooled reflux condenser and drying tube filled with Drierite desiccant. The reaction was stirred under reflux (~37° C.) for 16 hours. The methylene chloride solvent was removed in vacuo, leaving a slightly yellow, clear oil. The oil was taken up in 2 ml carbon tetrachloride and placed onto 7.8 g neutral alumina (pH 6.9) packed with carbon tetrachloride into a 15 ml "course" glass sintered funnel. The carbon tetrachloride was removed in vacuo, leaving 0.74 g of crude 2,2-dinitropropyl vinyl ether (IX) which was shown by nuclear resonance spectrometry to be 92 percent pure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04426540 |
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| Source dataset | uspto-grants-1984_01 |
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| ORD ID | ord-1d82b5865c2d44178bb960f121bc7a9a |
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| Source note | uspto-grants-1984_01 |
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