Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1524575Generated: October 25, 2026

Methyl iodide → 1-Bromo-5-(1,1-dimethoxyethyl)-2-methoxy-3-trifluoromethylbenzene

https://huagongshe.com/reaction/1524575

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantTrimethyl orthoformateHCID 9005—
ReactantPotassium CarbonateHCID 11430—
Reactant3'-Bromo-4'-hydroxy-5'-(trifluoromethyl)acetophenoneHCID 58085700—
CatalystD-Camphorsulfonic AcidHCID 65617—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
SolventHeptane waterHCID 57468513—
Product1-Bromo-5-(1,1-dimethoxyethyl)-2-methoxy-3-trifluoromethylbenzeneHCID 58085697—

Reaction Steps

1-(3-Bromo-4-hydroxy-5-trifluoromethylphenyl)ethanone (O4.004; 6.8 g) was dissolved in methanol (50 ml) and admixed successively with DL-10-camphorsulfonic acid (111 mg) and trimethyl orthoformate (8 ml). After stirring at RT for 2 h, DMF (75 ml), potassium carbonate (4.98 g) and then slowly, while cooling with ice, iodomethane (3 ml) were added. After stirring at RT for 4 h, the reaction mixture was left to stand overnight and then admixed with n-heptane/water, and the organic phase was removed. The aqueous phase was extracted by shaking once more with n-heptane, and the combined organic phases were then dried over magnesium sulfate, filtered and concentrated. 7 g of the title compound were obtained in sufficient purity.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09079906B2
Source datasetuspto-grants-2015_07
ORD IDord-25c7e30e53f64b27a6a56ce7c8000258
Source noteuspto-grants-2015_07