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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1646531Generated: November 1, 2026

Methyl iodide → HCID 13140128, compound

https://huagongshe.com/reaction/1646531

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantAcetonitrileHCID 6342—
ReactantSodium hydrideHCID 24758—
ReactantL-LeucinolHCID 111307—
SolventTetrahydrofuranHCID 8028—
ProductHCID 13140128HCID 13140128—

Reaction Conditions

Temperature55 °C

Reaction Steps

Sodium hydride (60% dispersion in oil: 9.39 g, 0.24 mol) was added to a stirred solution of L-leucinol (25 ml, 0.20 mol) in a mixture of dry acetonitrile (12 ml) and dry THF (60 ml) at room temperature under argon. The mixture was heated at reflux for 2 h, cooled to 55° C. and methyl iodide (12.8 ml, 2.1 mol) carefully added. The reaction mixture was heated at reflux overnight and allowed to cool to room temperature. Ice cold brine (100 ml) was added carefully and the mixture extracted with ethyl acetate (3×100 ml). The combined organic extracts were dried over anhydrous sodium sulphate, filtered and evaporated. The residue was distilled under reduced pressure to give (S)-1-isobutyl-2-methoxyethylamine as a colourless oil which was used directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05180723
Source datasetuspto-grants-1993_01
ORD IDord-ef7c01a8ae664b279c78a9fcaaf64f0e
Source noteuspto-grants-1993_01