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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1732751Generated: November 3, 2026

Methyl iodide → 2,3-Dihydro-4-hydroxy-7-methoxy-4-methyl-4H-1-benzopyran

https://huagongshe.com/reaction/1732751

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantAmmonium ChlorideHCID 25517—
Reactant7-methoxy-3,4-dihydro-2H-1-benzopyran-4-oneHCID 4387510—
ReactantMagnesiumHCID 5462224—
SolventDiethyl EtherHCID 3283—
Product2,3-Dihydro-4-hydroxy-7-methoxy-4-methyl-4H-1-benzopyranHCID 20304588—

Reaction Steps

Methyl iodide (145 g; 64.2 ml) in dry ether (50 ml) was added dropwise with stirring to magnesium turnings (22 g) in dry ether (730 ml). After the initial reaction had ceased the reaction mixture was refluxed for 1 hour, cooled and 2,3-dihydro-7-methoxy-4-oxo-4H-1-benzopyran, (77.9 g) in dry ether (440 ml) was added dropwise with stirring. After addition the reaction mixture was refluxed for 1 hour, cooled and the complex was decomposed by the addition of ammonium chloride solution. The ethereal layer was separated, washed with water and dried. Evaporation of the solvent left 76 g of the title compound as an oil (89%). MS and NMR analysis were correct for the required compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04238606
Source datasetuspto-grants-1980_12
ORD IDord-04305d7c45334004821ab4e9eff0a8c9
Source noteuspto-grants-1980_12