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HRID 390071Erstellt: 24. Oktober 2026
Benzylamine → (S)-N-benzyl-1-(2,2-dimethyl-1,3-dioxolan-4-yl)methanamine
https://huagongshe.com/de/reaction/390071
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Benzylamine | HCID 7504 | — |
| Edukt | (+)-Solketal | HCID 736057 | — |
| Edukt | HCID 15570842 | HCID 15570842 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | (S)-N-benzyl-1-(2,2-dimethyl-1,3-dioxolan-4-yl)methanamine | HCID 11042283 | 76% |
| Produkt | HCID 15570842 | HCID 15570842 | — |
Reaktionsschritte
(R)-(2,2-Dimethyl-1,3-dioxolan-4-yl)methyl methanesulfonate was prepared from (S)-(2,2-dimethyl-1,3-dioxolan-4-yl)methanol (Sigma-Aldrich, 99% ee) by a known literature procedure (H. S. Kim, D. Barak, T. K. Harden, J. L. Boyer and K. A. Jacobson, J. Med. Chem., 2001, 44, 3092). The title compound was prepared in the same way as described by M. Lemaire, F. Posada, J.-G. Gourcy and G. Jeminet, Synlett, 1995, 627. A solution of (R)-(2,2-dimethyl-1,3-dioxolan-4-yl)methyl methanesulfonate (3.9 g, 18.55 mmol) and benzylamine (8.10 ml, 74.2 mmol) was refluxed in CH3CN (50 ml) for 48 h. The solvent was evaporated and the residue dissolved in EtOAc and washed with aqueous sat. NaHCO3, dried and the solvent evaporated. The residue was chromatographed (EtOAc-hex, 6:4 then 8:2) to give (S)—N-benzyl-1-(2,2-dimethyl-1,3-dioxolan-4-yl)methanamine (3.1 g, 14.01 mmol, 76% yield) as a yellow oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08383636B2 |
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| Quelldatensatz | uspto-grants-2013_02 |
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| ORD ID | ord-2dafa71afaf54e4bb5b7cb2364c7cbdb |
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| Quellennotiz | uspto-grants-2013_02 |
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