HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 11209Erstellt: 24. Oktober 2026
Diethyl Ether → (2R,3R)-2-(3-chlorophenyl)-3,5,5-trimethyl-2-morpholinol
https://huagongshe.com/de/reaction/11209
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Diethyl Ether | HCID 3283 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | Bupropion Morpholinol (2R,3R)-Isomer | HCID 9943907 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | (2R,3R)-2-(3-chlorophenyl)-3,5,5-trimethyl-2-morpholinol | HCID 9943908 | — |
Reaktionsschritte
(+/−)-(2R*,3R*)-2-(3-chlorophenyl)-3,5,5-trimethyl-2-morpholinol hydrochloride may be converted back to its free base by the following process. A 3.0 g sample of (+/−)-(2R*,3R*)-2-(3-chlorophenyl)-3,5,5-trimethyl-2-morpholinol hydrochloride was dissolved in water (100 mL) and diethyl ether was added (200 mL). The mixture was chilled in an ice bath and the pH was adjusted to >10 with 1.0N aqueous sodium hydroxide. After stirring for 30 min., the phases were separated and the aqueous phase was extracted with diethyl ether. The combined diethyl ether extracts were dried (Na2SO4) and concentrated in vacuo to give 2.6 g of (+/−)-(2R*,3R*)-2-(3-chlorophenyl)-3,5,5-trimethyl-2-morpholinol as a white solid. This was used without further purification for the chiral chromatography described below.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07098206B2 |
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| Quelldatensatz | uspto-grants-2006_08 |
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| ORD ID | ord-ccf1d5796b1247748d63c86e697ede67 |
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| Quellennotiz | uspto-grants-2006_08 |
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