HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1817777Generated: November 1, 2026
Potassium Hydroxide → 4,5-Diacetyl-[1,4,5]-oxadiazepine
https://huagongshe.com/reaction/1817777
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Acetic acid, 2-acetylhydrazide | HCID 72884 | — |
| Reactant | 2,2-Dichlorodiethyl Ether | HCID 13987514 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4,5-Diacetyl-[1,4,5]-oxadiazepine | HCID 67335862 | — |
Reaction Steps
39.6 g of potassium hydroxide powder 85% (0.6 mol) are introduced into a mixture of 35 g of diacetylhydrazine (0.3 mol) and 560 ml of solvent (see Table 1). When the heat of reaction has died away, 85.8 g of 2,2-dichlorodiethyl ether (0.6 mol) are added; the reaction mixture is heated to 80° C. and maintained at 80-90° C. for 5 hours. The mixture is then cooled to 20° C. and filtered, and the filtration residue is washed with the solvent. The yield is given by the content of title compound in the combined filtrate. It will be seen that the solvents used according to the invention (tests 4-7) give far better yields of 4,5-diacetyl-[1,4,5]-oxadiazepine than N,N-dimethylformamide, which is known from the above prior art (DMFA, comparison test 8).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07598376B2 |
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| Source dataset | uspto-grants-2009_10 |
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| ORD ID | ord-49d7f6fdbc1545e7a7b36f289b6276b9 |
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| Source note | uspto-grants-2009_10 |
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