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HRID 390071作成日:2026年10月25日

Benzylamine → (S)-N-benzyl-1-(2,2-dimethyl-1,3-dioxolan-4-yl)methanamine

https://huagongshe.com/reaction/390071

反応式

関与物質

役割名称HCID仕込み量
反応物BenzylamineHCID 7504—
反応物(+)-SolketalHCID 736057—
反応物Methanesulfonic acid [(R)-2,2-dimethyl-[1,3]dioxolan-4-yl]methyl esterHCID 15570842—
溶媒AcetonitrileHCID 6342—
生成物(S)-N-benzyl-1-(2,2-dimethyl-1,3-dioxolan-4-yl)methanamineHCID 1104228376%
生成物Methanesulfonic acid [(R)-2,2-dimethyl-[1,3]dioxolan-4-yl]methyl esterHCID 15570842—

反応手順

(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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08383636B2
出典データセットuspto-grants-2013_02
ORD IDord-2dafa71afaf54e4bb5b7cb2364c7cbdb
出典メモuspto-grants-2013_02