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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 629184Generated: October 31, 2026

Iodine → 4-bromo-1-methyl-1H-pyrrole-2-carbaldehyde

https://huagongshe.com/reaction/629184

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant1-Methyl-1H-pyrrole-2-carbaldehydeHCID 14504—
ReactantBromineHCID 24408—
SolventChloroformHCID 6212—
Product4-bromo-1-methyl-1H-pyrrole-2-carbaldehydeHCID 1219670195.7%

Reaction Conditions

Temperature-10 °C

Reaction Steps

To a solution of 1-methyl-1H-pyrrole-2-carbaldehyde (1.09 g, 10.0 mmol) in 60 mL chloroform at −20° C. was added a single crystal of iodine. The mixture was stirred until homogeneous. Bromine (0.51 mL, 10.0 mmol) was added dropwise as a solution in 10 mL chloroform. The solution was stirred while warming from −20 to 0° C. over 1.5 h. Chloroform was removed in vacuo and the residue added to 5% sodium bisulfite solution to quench excess bromine/iodine. Saturated sodium bicarbonate was added until the pH of the mixture reached 7. Organics were extracted with ether (3×75 mL), dried over magnesium sulfate, filtered and concentrated to give crude 4-bromo-1-methyl-1H-pyrrole-2-carbaldehyde (1.80 g) as the major component of a mixture of starting aldehyde and dibromopyrrole. Used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09315495B2
Source datasetuspto-grants-2016_04
ORD IDord-d0a7cfb1dfa24d24a38fb0f2948c3489
Source noteuspto-grants-2016_04