HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1799784Generated: November 1, 2026
Bromine → 5-Bromo-3-methylthiophene-2-carbaldehyde
https://huagongshe.com/reaction/1799784
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 3-Methyl-2-thiophenecarboxaldehyde | HCID 79911 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Bromo-3-methylthiophene-2-carbaldehyde | HCID 15115407 | 95.1% |
Reaction Steps
Following the preparation as described in U.S. Publication No. 2006/0199836, Br2 (3.67 mL, 71.3 mmol) was added to a solution of 3-methylthiophene-2-carbaldehyde (8.55 mL, 71.3 mmol) in chloroform (59.4 mL) dropwise at 0° C. over a period of 20 min. The reaction was allowed to slowly warm to room temperature and stir for 2 h. The brown/red solution was diluted with 150 mL of CH2Cl2 and washed with water, 1.5 M K2HPO4 and brine. The organic layer was dried over anhydrous Na2SO4 and concentrated. The residue was purified by flash chromatography (silica gel, hexanes:EtOAc, 100:0 to 50:50) to afford 13.9 g (72% yield) of the title compound as a brown solid: 1H NMR (400 MHz, CDCl3) δ 9.91 (s, 1H), 6.97 (s, 1H), 2.54 (s, 3H); HPLC retention time: 2.718 min., LCMS (ES): m/z 207 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08344160B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-c657776d4b204165821a1e4dfb5b3cf0 |
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| Source note | uspto-grants-2013_01 |
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