HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 543575Erstellt: 25. Oktober 2026
Chloroform → 2-Chloro-1-(isoxazolidin-2-yl)propan-1-one
https://huagongshe.com/reaction/543575
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Chloroform | HCID 6212 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 2-Chloropropionyl chloride | HCID 111019 | — |
| Edukt | Isoxazolidine hydrochloride | HCID 12304500 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 2-Chloro-1-(isoxazolidin-2-yl)propan-1-one | HCID 13314616 | 91,3% |
Reaktionsschritte
To a mixture of isoxazolidine hydrochloride (11.0 g) and chloroform (200 ml) was added (±)-2-chloropropionyl chloride (13.3 g) under ice-cooling and stirring and then added dropwise triethylamine (22.2 g) under the same conditions. The stirring was continued at room temperature for further one hour, after which an amount of water was added to the reaction mixture to form layers. The organic layer thus separated was washed with 1 N hydrochloric acid and then with a 5% aqueous sodium bicarbonate solution and dried over anhydrous sodium sulfate. Removal of the solvent by a distillation in vacuo gave N-[(±)-2-chloropropionyl]isoxazolidine (15.0 g) as a pale yellow oil. Purification of the oil by silica gel column chromatography afforded a colorless oil. nD20 =1.4918.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04447259 |
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| Quelldatensatz | uspto-grants-1984_05 |
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| ORD ID | ord-a2395f5bbfa940c9a5a470319191bb8c |
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| Quellennotiz | uspto-grants-1984_05 |
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