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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1720109Generated: October 30, 2026

Iodine → HCID 19783693, compound

https://huagongshe.com/reaction/1720109

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant1-Bromo-2,5-dimethoxy-3,4,6-trimethylbenzeneHCID 297365—
ReactantMagnesiumHCID 5462224—
CatalystMethyl iodideHCID 6328—
SolventTetrahydrofuranHCID 8028—
ProductHCID 19783693HCID 19783693—

Reaction Steps

In an atmosphere of an argon stream, 1.1 g (0.045 mol) of magnesium, one drop of methyl iodide, and a catalytic amount of iodine were added to 30 ml of tetrahydrofuran, and further, a solution of 10.4 g (0.04 mol) of 2,5-dimethoxy-3,4,6-trimethyl-bromobenzene in 15 ml of tetrahydrofuran was added dropwise over 40 minutes while refluxing the tetrahydrofuran. The reaction was completed by refluxing for further 30 minutes, to thereby form 2,5-dimethoxy-3,4,6-trimethylbenzene magnesium bromide. Then, after cooling to 0° C., 580 mg (4.4 mmol) of the lactol compound (102) prepared in Example 1 was added and stirred at a room temperature for 2 hours, an aqueous sodium bicarbonate saturated solution was added to the reaction mixture, and an extraction with diethyl ether was carried out. The organic phase was washed with an aqueous sodium chloride saturated solution, and dried over anhydrous magnesium sulfate, the solvent was evaporated under a reduced pressure, and the residue was treated by silica gel column chromatography. Then, 1.35 g (98.5%) of the above-mentioned compound (103) was obtained from the ethyl acetate effluent as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05504219
Source datasetuspto-grants-1996_04
ORD IDord-2131b66ce80b48e2896ef24711f22530
Source noteuspto-grants-1996_04