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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453565Generated: October 27, 2026

Bromine → 4-Bromo-5-methylthiophene-2-carbaldehyde

https://huagongshe.com/reaction/453565

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
Reactant5-Methyl-2-thiophenecarboxaldehydeHCID 61663—
ReactantSodium BicarbonateHCID 516892—
SolventAcetic AcidHCID 176—
Product4-Bromo-5-methylthiophene-2-carbaldehydeHCID 1553821250%

Reaction Steps

To a solution of 5-methylthiophene-2-carbaldehyde (50.0 g) in acetic acid (400 mL) was added dropwise a solution of bromine (25 mL) in acetic acid (200 mL) at room temperature over 6 hr. After the dropwise addition, the reaction mixture was stirred overnight, neutralized with saturated aqueous sodium hydrogen carbonate solution, and extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried (MgSO4) and concentrated. The obtained residue was dissolved in toluene (50 mL), and the mixture was stirred at 110° C. for 2 hr and concentrated. The residue was subjected to silica gel column chromatography, eluted with ethyl acetate-hexane (1:5, volume ratio) and concentrated to give 4-bromo-5-methylthiophene-2-carbaldehyde (40.0 g, yield 50%) as yellow crystals. melting point 60° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492405B2
Source datasetuspto-grants-2013_07
ORD IDord-a5c4e52c31994f848de269f47521ebcb
Source noteuspto-grants-2013_07