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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1722385Generated: October 31, 2026

Sodium Iodide → 7-Methoxy-2-(5-methoxyhept-1-y)bicyclo[3.3.0]octane

https://huagongshe.com/reaction/1722385

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantMethyl iodideHCID 6328—
ReactantOctahydro-4-(5-methoxyheptyl)-2-pentalenolHCID 15053012—
Reactant2-(5-Methoxyhept-1-yl)bicyclo[3.3.0]octanolHCID 20028717—
SolventTetrahydrofuranHCID 8028—
Product7-Methoxy-2-(5-methoxyhept-1-y)bicyclo[3.3.0]octaneHCID 15053047—

Reaction Conditions

Temperature50 °C

Reaction Steps

The starting material, 2-(5-methoxyhept-1-yl)bicyclo[3.3.0]octanol {octahydro-4-(5-methoxyheptyl)-2-pentalenol} (1.0 g, 3.9 mmoles) is added to a reaction vessel containing sodium iodide (0.12 g, 4.9 mmoles) and tetrahydrofuran (12 ml). The solution is stirred while methyl iodide (0.84 g, 5.9 mmoles) is rapidly added. The reaction is heated in a 50° C. water bath for 4 hours. The water bath is removed and the reaction neutralized with the addition of water (5 ml). The organic phase is separated and the aqueous phase extracted with ether (2×50 ml). The ether extracts are combined and washed with brine (50 ml). The solution is dried over anhydrous magnesium sulfate and the solvent removed under vacuum leaving a clear yellow oil. The product is then kugelrohred under reduced pressure leaving a pale yellow oil (0.8 g, 3.1 mmoles).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04855322
Source datasetuspto-grants-1989_08
ORD IDord-2f68bce189284e71b6a32b3dcfcc9d01
Source noteuspto-grants-1989_08