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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1039643Generated: October 31, 2026

Methyl iodide → (4-Methyloxan-4-yl)methanamine

https://huagongshe.com/reaction/1039643

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantOxane-4-carbonitrileHCID 11815837—
SolventTetrahydrofuranHCID 8028—
Product(4-Methyloxan-4-yl)methanamineHCID 54165201—

Reaction Steps

A mixture of tetrahydropyran-4-carbonitrile (5.00 g) and THF (50 ml) was admixed at 0° C. with lithium hexamethyldisilazide (1 M, 63 ml) and, after 90 minutes, methyl iodide (4.26 ml) was added dropwise with good cooling. After 12 hours, the reaction mixture was partitioned between water and ethyl acetate. The organic phase was dried over sodium sulfate and concentrated. The residue was dissolved in THF (200 ml), and lithium aluminum hydride (3.79 g) was added. The mixture was boiled at reflux for 6 hours. Water (3.8 ml) and then sodium hydroxide solution (40%; 3.8 ml) were cautiously added dropwise to the cooled suspension. The precipitate was filtered off and the filtrate was concentrated. This afforded the product with the molecular weight of 129.20 (C7H15NO); MS (ESI): 130 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08552199B2
Source datasetuspto-grants-2013_10
ORD IDord-ed8e2eb06d154167a8247f75120ff5ca
Source noteuspto-grants-2013_10