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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 390071생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/390071

반응식

참여 물질

역할이름HCID투입량
반응물BenzylamineHCID 7504—
반응물(+)-SolketalHCID 736057—
반응물HCID 15570842HCID 15570842—
용매AcetonitrileHCID 6342—
생성물(S)-N-benzyl-1-(2,2-dimethyl-1,3-dioxolan-4-yl)methanamineHCID 1104228376%
생성물HCID 15570842HCID 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08383636B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-2dafa71afaf54e4bb5b7cb2364c7cbdb
출처 메모uspto-grants-2013_02