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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 435779Generated: October 29, 2026

Methyl iodide → 1,1,5-Trimethoxy-2,6-dimethylheptane

https://huagongshe.com/reaction/435779

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant7,7-Dimethoxy-2,6-dimethylheptan-3-olHCID 21399162—
ReactantHCID 178418361HCID 178418361—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventHexamethylphosphoramideHCID 12679—
Product1,1,5-Trimethoxy-2,6-dimethylheptaneHCID 21399064—

Reaction Steps

To a mixture of 2.4 g. of clean sodium hydride in 200 ml. of dry tetrahydrofuran containing 20 ml. of dry HMPT (hexamethylphosphorictriamide) is added dropwise a solution of 20.4 g. of 1,1-dimethoxy-5-hydroxy-2,6-dimethylheptane in dry tetrahydrofuran. The mixture is stirred at room temperature until evolution of hydrogen ceases and then 16 g. of methyl iodide is added. The reaction mixture is refluxed for 3 hours and then cooled, diluted with water and extracted with ether. The etheral extracts are evaporated under reduced pressure to yield crude 1,1,5-trimethoxy-2,6-dimethylheptane which can be purified by distillation or chromatography on Florisil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04006188
Source datasetuspto-grants-1977_02
ORD IDord-1a674a57c5a64207b846afc4c8e91644
Source noteuspto-grants-1977_02