HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 978704Erstellt: 25. Oktober 2026
Hydrochloric Acid → [1-Benzyl-3-(hydroxymethyl)azetidin-3-YL]methanol
https://huagongshe.com/reaction/978704
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Benzylamine | HCID 7504 | — |
| Edukt | [3-(Bromomethyl)oxetan-3-yl]methanol | HCID 529264 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | [1-Benzyl-3-(hydroxymethyl)azetidin-3-YL]methanol | HCID 20164320 | — |
Reaktionsschritte
18.1 g of 1A and 11.7 g of benzylamine were mixed with 5 ml of water and the resulting mixture was stirred at 100° C. After 4 hours the solution was allowed to cool to ambient temperature and 13.8 ml of 36% (w/w) hydrochloric acid was added. The resulting mixture was stirred at 60° C. After 2 hours the solution was again allowed to cool to room temperature and then washed with dichloromethane to remove by-products. The aqueous layer was made alkaline by the addition of a solution of 5.5 g of sodium hydroxide in 10 ml of water and stirred at 100° C. for 1 hour. After cooling to ambient temperature the pH of the mixture was raised by addition of another solution of 5.5 g of sodium hydroxide in 10 ml of water and washed with hexane to remove benzylamine. The water was evaporated under reduced pressure, and the solid residue was taken up in dichloromethane. Inorganic salts, which remained undissolved, were removed by filtration, and the dichloromethane was evaporated in vacuo, leaving 1, as a white crystalline solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04665197 |
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| Quelldatensatz | uspto-grants-1987_05 |
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| ORD ID | ord-c4cd9b50b8c84c5e8537f76c629da15e |
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| Quellennotiz | uspto-grants-1987_05 |
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