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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | HCID 22930050 | HCID 22930050 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5-bromo-3-tert-butyl-2-hydroxybenzaldehyde | HCID 797006 | 111% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07244730B2 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-3b9cde35ea9f4b3fb439de6be3084343 |
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| Source note | uspto-grants-2007_07 |
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