참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Benzylamine | HCID 7504 | — |
| 반응물 | (+)-Solketal | HCID 736057 | — |
| 반응물 | HCID 15570842 | HCID 15570842 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | (S)-N-benzyl-1-(2,2-dimethyl-1,3-dioxolan-4-yl)methanamine | HCID 11042283 | 76% |
| 생성물 | HCID 15570842 | HCID 15570842 | — |
반응 단계
(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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08383636B2 |
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| 출처 데이터셋 | uspto-grants-2013_02 |
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| ORD ID | ord-2dafa71afaf54e4bb5b7cb2364c7cbdb |
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| 출처 메모 | uspto-grants-2013_02 |
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