Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1526773Generated: November 4, 2026

Potassium Carbonate → HCID 86709940, compound

https://huagongshe.com/reaction/1526773

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-(Chloromethoxy)-2-methoxyethaneHCID 77590—
Reactant5-bromo-3-tert-butyl-2-hydroxybenzaldehydeHCID 797006—
SolventDimethylformamideHCID 6228—
ProductHCID 86709940HCID 86709940106.7%

Reaction Conditions

Temperature20 °C

Reaction Steps

A mixture of 5-bromo-3-(tert-butyl)-2-hydroxybenzaldehyde (4.74 g, 18.42 mmol) and anhydrous potassium carbonate (2.83 g, 20.45 mmol) in anhydrous DMF (20.0 mL) was stirred under nitrogen in a water bath (20° C.) to give an orange-yellow suspension. After stirring for 20 min, 2-methoxyethoxymethyl chloride (2.40 mL, 21.19 mmol, technical grade) was added drop wise (20 min) to above suspension while maintaining an internal temperature of 20° C. The reaction mixture was stirred at room temperature for 3 h to give a canary yellow suspension. The reaction mixture was poured into ice-water (150 mL) and stirred at room temperature to give a yellow oily liquid, no solid formation was observed. After 30 min of stirring, the reaction mixture was extracted with dichloromethane (2×75 mL). The organic layer was removed, washed with water (1×50 mL) and dried over anhydrous magnesium sulfate, filtered and evaporated in-vacuo to give a pale yellow viscous liquid (6.7832 g). No purification was necessary and the crude product (purity >97%) was used directly in the next Step #3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09085606B2
Source datasetuspto-grants-2015_07
ORD IDord-43a66aeefbcc4257b1ffac18684dea89
Source noteuspto-grants-2015_07