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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 390071Generated: October 26, 2026

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

https://huagongshe.com/reaction/390071

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylamineHCID 7504—
Reactant(+)-SolketalHCID 736057—
ReactantMethanesulfonic acid [(R)-2,2-dimethyl-[1,3]dioxolan-4-yl]methyl esterHCID 15570842—
SolventAcetonitrileHCID 6342—
Product(S)-N-benzyl-1-(2,2-dimethyl-1,3-dioxolan-4-yl)methanamineHCID 1104228376%
ProductMethanesulfonic acid [(R)-2,2-dimethyl-[1,3]dioxolan-4-yl]methyl esterHCID 15570842—

Reaction Steps

(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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383636B2
Source datasetuspto-grants-2013_02
ORD IDord-2dafa71afaf54e4bb5b7cb2364c7cbdb
Source noteuspto-grants-2013_02