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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2068871Generated: October 31, 2026

Methyl iodide → 7-Methyl-1,4-dioxaspiro[4.5]decan-8-one

https://huagongshe.com/reaction/2068871

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantAmmonium ChlorideHCID 25517—
Reactant1,4-Dioxaspiro[4.5]decan-8-oneHCID 567415—
ReactantLithium HexamethyldisilazideHCID 2733832—
SolventTetrahydrofuranHCID 8028—
Product7-Methyl-1,4-dioxaspiro[4.5]decan-8-oneHCID 27062862.3%

Reaction Steps

Under a nitrogen atmosphere, to a solution of lithium bis(trimethylsilyl)amide (1M, 100 ml, 100 mmol) in tetrahydrofuran (200 ml) was added dropwise a solution of 1,4-dioxaspiro[4.5]decan-8-one (15.6 g, 100 mmol) in tetrahydrofuran (50 ml) at −78° C. over about 30 min, and the mixture was stirred for 30 min. Then, methyl iodide (2.5 ml, 120 mmol) was added dropwise over 5 min, and the mixture was stirred at −78° C. for 30 min, and at room temperature for 2 hr. To the reaction mixture was added saturated aqueous ammonium chloride solution, and the mixture was extracted three times with diethyl ether. The combined organic layers were dried over magnesium sulfate. Magnesium sulfate was removed by filtration, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel chromatography to give the title compound (10.6 g, yield 62%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299070B2
Source datasetuspto-grants-2012_10
ORD IDord-d9e3628c2343459f9827cf54cd27a9cc
Source noteuspto-grants-2012_10