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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1970975Generated: October 26, 2026

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

https://huagongshe.com/reaction/1970975

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantAmmonium ChlorideHCID 25517—
Reactant1,4-Dioxaspiro[4.5]decan-8-oneHCID 567415—
ReactantLithium HexamethyldisilazideHCID 2733832—
SolventDimethylformamideHCID 6228—
Solventtert-Butyl methyl etherHCID 15413—
Product7-Methyl-1,4-dioxaspiro[4.5]decan-8-oneHCID 270628—

Reaction Conditions

Temperature-60 °C

Reaction Steps

To a stirred solution of LHMDS (1.0 M in THF, 2.1 L, 2.1 mol) at −60° C. was added 1,4-dioxaspiro[4.5]decan-8-one (300 g, 1.9 mol) in DMF (1.2 L) slowly via an addition funnel while maintaining the reaction temperature below −60° C. The reaction mixture was allowed to stir at −60° C. for 1.5 h, and treated with MeI (286 g, 2.0 mol) via an addition funnel. The reaction mixture was allowed to warm to room temperature over 3 h, and treated with half-saturated ammonium chloride solution (2 L). The mixture was diluted with MTBE (2 L), washed with water (×3), dried (magnesium sulfate), and concentrated. The residue was azeotroped with isooctane (500 mL×2), and recrystallized from isooctane to afford the title compound. 1H NMR (400 MHz, CDCl3) δ 4.05-3.95 (m, 4H); 2.70 (m, 1H); 2.61 (dtd, 1H); 2.33 (ddd, 1H); 2.10-1.97 (m, 2H); 1.92 (dt, 1H); 1.68 (t, 1H); 1.00 (d, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431569B2
Source datasetuspto-grants-2013_04
ORD IDord-bf43feb564db4cfca03c48f1e1befdbc
Source noteuspto-grants-2013_04