Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1524567Generated: November 3, 2026

Bromide ion → 1-[3-Tert-butyl-5-(3-hydroxy-2,2-dimethylpropoxy)-4-methoxyphenyl]ethanone

https://huagongshe.com/reaction/1524567

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromide ionHCID 259—
ReactantCesium carbonateHCID 10796—
Reactant3-Bromo-2,2-dimethylpropyl acetateHCID 13357715—
Reactant1-(3-Tert-butyl-5-hydroxy-4-methoxyphenyl)ethanoneHCID 58136946—
SolventDimethylformamideHCID 6228—
Product1-[3-Tert-butyl-5-(3-hydroxy-2,2-dimethylpropoxy)-4-methoxyphenyl]ethanoneHCID 5804588142.2%

Reaction Conditions

Temperature150 °C

Reaction Steps

1-(3-tert-Butyl-5-hydroxy-4-methoxyphenyl)ethanone (O3.070; 2.00 g) and 3-bromo-2,2-dimethylpropyl acetate (2.54 g) were dissolved in DMF (15 ml), and cesium carbonate (3.69 g) was added. After stirring at 150° C. and max. 15 bar in a microwave for 2.5 h, a further 0.5 eq. of the bromide was added and the mixture was placed into the microwave at 150° C. for a further 2 h. Then the mixture was concentrated by rotary evaporation and the residue was partitioned between DCM and water. The DCM phase was removed, dried over magnesium sulfate, filtered and concentrated. The residue was purified using silica gel (120 g cartridge, n-heptane/MtB ether gradient of 0-50% within 60 min). 1.17 g of the title compound were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09079906B2
Source datasetuspto-grants-2015_07
ORD IDord-87260c9397574af2be29605d307bea42
Source noteuspto-grants-2015_07