HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 72423Erstellt: 24. Oktober 2026
1-Chloroethyl chloroformate → 3-(4-Fluorophenoxy)azetidine
https://huagongshe.com/de/reaction/72423
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1-Chloroethyl chloroformate | HCID 521305 | — |
| Edukt | 1-Benzhydryl-3-(4-fluorophenoxy)azetidine | HCID 15053369 | — |
| Lösungsmittel | 1,2-Dichloroethane | HCID 11 | — |
| Produkt | 3-(4-Fluorophenoxy)azetidine | HCID 21428730 | 99,9% |
Reaktionsschritte
1-chloroethyl chloroformate (0.87 ml, 8.09 mmol) was added to an ice-cooled solution of 1-benzhydryl-3-(4-fluorophenoxy)azetidine (D21) (1.8 g, 5.39 mmol) in 1,2 dichloroethane (18 ml) and the resulting mixture was heated under reflux for 3 hours. The reaction mixture was evaporated in vacuo and the residue was re-dissolved in methanol (10 ml). This solution was heated under reflux overnight then cooled at room temperature and evaporated in vacuo. The obtained residue was loaded on SPE-SCX (20 g) cartridge. The ammonia fractions, after evaporation in vacuo, were loaded on by SPE-Si (5 g) cartridge eluting with a mixture dichloromethane/dichloromethane:NH3 (2M solution in MeOH) (from 100/0 to 80/20). Collected fractions after solvent evaporation afforded the title compound (D49) (0.9 g)
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08828987B2 |
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| Quelldatensatz | uspto-grants-2014_09 |
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| ORD ID | ord-c055887e6a81427db20809de6ebda7cf |
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| Quellennotiz | uspto-grants-2014_09 |
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