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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2214124Generated: October 30, 2026

Sodium Iodide → 8-(Iodomethyl)-1,4-dioxaspiro[4.5]decane

https://huagongshe.com/reaction/2214124

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
Reactant1,4-Dioxaspiro[4.5]decan-8-ylmethanolHCID 10080838—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product8-(Iodomethyl)-1,4-dioxaspiro[4.5]decaneHCID 2195905888.6%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of (1,4-dioxa-spiro[4.5]dec-8-yl)-methanol (1.60 g, 9.29 mmol) in methylene chloride (50 mL) was treated with 4-(dimethylamino)pyridine (1.26 g, 10.22 mmol) and p-toluenesulfonyl chloride (1.86 g, 9.75 mmol). The reaction mixture was stirred at 25° C. for 2 h, and was then washed with a saturated aqueous sodium bicarbonate solution (1×25 mL). The organic layer was dried over magnesium sulfate, filtered, and concentrated in vacuo. The resulting oil was dissolved in acetone (30 mL) and treated with sodium iodide (4.73 g, 31.53 mmol). The reaction was heated under reflux for 2 h, cooled to 25° C., and then concentrated in vacuo. The resulting residue was suspended in ethyl acetate (50 mL), washed with water (2×15 mL), dried over magnesium sulfate, filtered, and concentrated in vacuo. Biotage chromatography (FLASH 40S, Silica, 19/1 hexanes/ethyl acetate) afforded 8-iodomethyl-1,4-dioxa-spiro[4.5]decane (2.32 g, 88.6%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07105671B2
Source datasetuspto-grants-2006_09
ORD IDord-48e41507e09b4605ab4d855dd1c0af6e
Source noteuspto-grants-2006_09