HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2040932Erstellt: 25. Oktober 2026
Hydrochloric Acid → 3-[2-(4-Chlorophenoxy)phenyl]-4-hydroxy-1-methylpyrrolidine-2-one
https://huagongshe.com/reaction/2040932
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | Potassium borohydride | HCID 4192641 | — |
| Edukt | 3-(2-(4-Chlorophenoxy)phenyl)-1-methylpyrrolidine-2,4-dione | HCID 23148658 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 3-[2-(4-Chlorophenoxy)phenyl]-4-hydroxy-1-methylpyrrolidine-2-one | HCID 67979731 | 89,6% |
Reaktionsschritte
5 g (15.8 mmol) of 3-[2-(4-chlorophenoxy)phenyl]-1-methylpyrrolidine-2,4-dione (compound IVb) was dissolved in a mixture of 150 mL of tetrahydrofuran and 15 mL of water. The solution was cooled to 0° C., and 4.3 g of potassium borohydride were added slowly, keeping the temperature below 10° C. The resulting solution was stirred at 0° C. for 6 hours. Then, a saturated solution of ammonium chloride was added, and the pH was adjusted to 3 with HCl 2 M. 100 mL of ethyl acetate were added. The organic phase was extracted, washed with saturated sodium bicarbonate and with water, dried and concentrated under vacuum, to obtain 4.5 g of 3-[2-(4-chlorophenoxy)phenyl]-4-hydroxy-1-methylpyrrolidine-2-one (compound XIIIb) as a sticky solid. Yield: 89.6%.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08580972B2 |
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| Quelldatensatz | uspto-grants-2013_11 |
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| ORD ID | ord-d3b23bfebb624a09bb92814f10e4d986 |
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| Quellennotiz | uspto-grants-2013_11 |
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