HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1975Erstellt: 23. Oktober 2026
Hydrochloric Acid → tetraethyl N-benzyl-5-aminopentane-1,1-bisphosphonate
https://huagongshe.com/de/reaction/1975
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | (Dimethyl sulfide)trihydroboron | HCID 12423031 | — |
| Edukt | tetraethyl N-benzoyl-5-aminopentane-1,1-bisphosphonate | HCID 19689031 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | tetraethyl N-benzyl-5-aminopentane-1,1-bisphosphonate | HCID 19689058 | 45,8% |
Reaktionsschritte
A solution of tetraethyl N-benzoyl-5-aminopentane-1,1-bisphosphonate (0.63 g, 1.36 mmol) in THF (3.4 mL) was cooled to 0° C., and borane methylsulfide (0.34 ml, 3.4 mmol) was added via syringe. The reaction was stirred at 0° C. for 20 minutes, then warmed to 65° C. for 2.5 hours. The reaction mixture was cooled to 0° C. and 6N HCl (4.0 ml) was added carefully. The solvent was removed in vacuo, and the residue was concentrated repeatedly from methanol (2×5 mL). The residue was dissolved in water (10 ml) and extracted with diethyl ether (3×5 ml). The aqueous layer was made basic to phenolphthalein with solid KOH and saturated with NaCl. The product was extracted into dichloromethane (5×20 ml), dried (Na2SO4) and concentrated to give the title compound (0.28 g).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05728650 |
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| Quelldatensatz | uspto-grants-1998_03 |
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| ORD ID | ord-861d1c5c6eb14e7f813a68ed25b21881 |
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| Quellennotiz | uspto-grants-1998_03 |
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