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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1414831Generated: November 1, 2026

Methyl iodide → 6-[(6-Methoxy-3,7,7-trimethyloct-2-en-1-yl)oxy]-2,3-dihydro-1-benzofuran

https://huagongshe.com/reaction/1414831

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium hydrideHCID 24758—
Reactant6-[(6-Hydroxy-3,7,7-trimethyl-2-octenyl)-oxy]-2,3-dihydrobenzofuranHCID 53891706—
SolventHexamethylphosphoramideHCID 12679—
Product6-[(6-Methoxy-3,7,7-trimethyloct-2-en-1-yl)oxy]-2,3-dihydro-1-benzofuranHCID 53713182—

Reaction Conditions

Temperature40 °C

Reaction Steps

0.4 g. of 6-[(6-hydroxy-3,7,7-trimethyl-2-octenyl)-oxy]-2,3-dihydrobenzofuran are dissolved in 10 ml. of absolute tetrahydrofuran and, while stirring, warmed to 40° C. for 2 hours with 0.5 g. of a 55% by weight sodium hydride suspension in oil. Then 2 ml. of hexamethylphosphoric acid triamide and 1 ml. of methyl iodide are added and the mixture is stirred for 12 hours at room temperature. For the working up, the mixture is poured onto ice-water and extracted twice with diethyl ether. The ether extracts are washed with water and saturated aqueous sodium chloride solution, dried over sodium sulfate and evaporated. By chromatography on silica gel with hexane/diethyl ether (19:1 parts by volume) there is obtained 6-[(6-methoxy-3,7,7-trimethyl-2-octenyl)-oxy]-2,3-dihydrobenzofuran; nD25 = 1.5170.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04002647
Source datasetuspto-grants-1977_01
ORD IDord-274842afeed347d5824f8787e5d4a7f4
Source noteuspto-grants-1977_01