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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1296019Generated: October 30, 2026

Bromine → 5-bromo-3-tert-butyl-2-hydroxybenzaldehyde

https://huagongshe.com/reaction/1296019

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantHCID 22930050HCID 22930050—
SolventMethanolHCID 887—
Product5-bromo-3-tert-butyl-2-hydroxybenzaldehydeHCID 797006111%

Reaction Conditions

Temperature20 °C

Reaction Steps

Bromine (747 g) was gradually added to a solution of the 3-(tert-butyl)-2-(methoxymethoxy)benzaldehyde (1247 g, 4.67 mol) in methanol (4000 ml) while cooling on ice. After stirring at 20° C. for 1 hour, the solvent was distilled off under reduced pressure, ethyl acetate was added to the residue, the mixture was washed with water, saturated sodium aqueous hydrogencarbonate and brine in that order and the organic layer was dried over anhydrous magnesium sulfate. The organic layer was concentrated under reduced pressure to yield a crude product of the title compound (1333 g) as a red oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07244730B2
Source datasetuspto-grants-2007_07
ORD IDord-3b9cde35ea9f4b3fb439de6be3084343
Source noteuspto-grants-2007_07