HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1817775Generated: November 2, 2026
Bis(2-chloroethyl) ether → 4,5-Diacetyl-[1,4,5]-oxadiazepine
https://huagongshe.com/reaction/1817775
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bis(2-chloroethyl) ether | HCID 8115 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Acetic acid, 2-acetylhydrazide | HCID 72884 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 4,5-Diacetyl-[1,4,5]-oxadiazepine | HCID 67335862 | 78.1% |
Reaction Steps
10.6 g of finely pulverised 85% potassium hydroxide are introduced into a solution of 9.3 g of N,N′-diacetylhydrazine and 141 g of dimethyl sulfoxide in such a manner that a temperature of 33° C. is not exceeded. After heating to 80 to 85° C., 23 g of 2,2′-dichlorodiethyl ether are added dropwise to the reaction mixture over the course of 50 minutes. The resulting highly fluid suspension is maintained at 80 to 85° C. for 3 hours, then cooled to 20 to 25° C. and filtered, and the filtration residue is washed with dimethyl sulfoxide. 11.4 g (76.0%) of 4,5-diacetyl-[1,4,5]-oxadiazepine are obtained from the combined filtrates by concentration by evaporation.
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-37d6fbc9fc80427a9f467d10f4be6b67 |
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| Source note | uspto-grants-2009_10 |
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