HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1781989Erstellt: 25. Oktober 2026
Hydrochloric Acid → 2-Methoxyestra-1,3,5(10)-triene-3-ol
https://huagongshe.com/reaction/1781989
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Potassium Hydroxide | HCID 14797 | — |
| Edukt | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Edukt | 2-Methoxyestrone | HCID 440624 | — |
| Lösungsmittel | Ethylene Glycol | HCID 174 | — |
| Lösungsmittel | 1-Butanol | HCID 263 | — |
| Produkt | 2-Methoxyestra-1,3,5(10)-triene-3-ol | HCID 46227378 | 72% |
Reaktionsschritte
2-Methoxyestrone (Scheme 1, Compound 4) (450 mg, 1.5 mmol) was suspended in ethylene glycol (10 mL) and n-butanol (2 mL). Hydrazine hydrate (0.145 mL, 3 mmol) was added and the mixture was heated to 130° C. for 1 h. The reaction was cooled to 70° C., KOH (253 mg, 4.5 mmol) was added, then the reaction was heated at 200° C. for 1 h. The mixture was cooled to room temperature, poured into ice and HCl (6N, 6 mL) was added. The resulting solid was filtered off. The solid was dissolved in acetone, which was then evaporated to give a product (Scheme 1, Compound 7) (310 mg, 72% yield). 1H NMR (300 MHz, CDCl3) δ 6.93 (1H, s, aromatic), 6.75 (1H, s, aromatic), 5.35 (1H, s, phenol), 3.95 (3H, s, methoxy), 2.95 (2H, dd, J=5.0, 3.0 Hz), 2.25 (2H, m,), 1.95 (2H, m), 1.95-1.05 (11H, m), 0.8 (3H, s)
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US07498322B2 |
|---|
| Quelldatensatz | uspto-grants-2009_03 |
|---|
| ORD ID | ord-b3178f60b4774d0b9e3efc65f3fe44ff |
|---|
| Quellennotiz | uspto-grants-2009_03 |
|---|