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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1884916Generated: November 3, 2026

Water → 5-Bromo-6,6'-dimethyl-2,2', 3', 4'-tetramethoxybenz-hydryl alcohol

https://huagongshe.com/reaction/1884916

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1,2-DibromoethaneHCID 7839—
Reactant3-Bromo-6-methoxy-2-methylbenzaldehydeHCID 11241668—
Reactant2-Bromo-3,4,5-trimethoxytolueneHCID 11436906—
SolventTetrahydrofuranHCID 8028—
Product5-Bromo-6,6'-dimethyl-2,2', 3', 4'-tetramethoxybenz-hydryl alcoholHCID 1121205159.7%

Reaction Conditions

Temperature30 °C

Reaction Steps

2.36 g of 2,3,4-trimethoxy-6-methylbromobenzene and 0.32 g of agnesium turnings were initially charged in 5 ml of anhydrous tetrahydrofuran, 0.57 ml of 1,2-dibromoethane was added and the reaction mixture was heated at reflux temperature for about 40 min. After cooling to 30° C., 1.40 g of 5-bromo-2-methoxy-6-methylbenzaldehyde were added dropwise, and the solution was stirred for about two hours. Water/2N hydrochloric acid (1/1) was added, the aqueous phase was extracted with ethyl acetate, the organic phases were washed with water and dried and the solvent was distilled off, and the residue was then purified by column chromatography (mobile phase petroleum ether/ethyl acetate 85/5). 1.5 g of the title compound were isolated as a violet viscous oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06767923B2
Source datasetuspto-grants-2004_07
ORD IDord-9cadd0e38ce64128bee78903c376aa78
Source noteuspto-grants-2004_07