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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | 1-Methyl-1H-pyrrole-2-carbaldehyde | HCID 14504 | — |
| Reactant | Bromine | HCID 24408 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 4-bromo-1-methyl-1H-pyrrole-2-carbaldehyde | HCID 12196701 | 95.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09315495B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-d0a7cfb1dfa24d24a38fb0f2948c3489 |
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| Source note | uspto-grants-2016_04 |
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