HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1441973Generated: October 30, 2026
2-Methylbenzaldehyde → 5-Bromo-2-methylbenzaldehyde
https://huagongshe.com/reaction/1441973
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Methylbenzaldehyde | HCID 10722 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Bromo-2-methylbenzaldehyde | HCID 10420289 | — |
Reaction Steps
77.7 g (583 mmol) of aluminium trichloride are suspended in 200 ml of dichloromethane and cooled to 0° C. 40.0 g (333 mmol) of 2-methylbenzaldehyde are added dropwise over the course of 30 min. Then 53.2 g (333 mmol) of bromine are added at 0° C. over the course of 6 h, and the mixture is allowed to warm to RT and is stirred for 12 h. The reaction solution is added to 500 ml of ice-water. The aqueous phase is extracted several times with dichloromethane. The combined organic phases are washed successively with 2N hydrochloric acid, a saturated aqueous sodium bicarbonate solution and a saturated aqueous sodium chloride solution. The organic phase is dried over sodium sulfate and concentrated in vacuo. Purification is by silica gel chromatography and subsequently by crystallization from cyclohexane. The precipitated product is filtered off.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07655643B2 |
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| Source dataset | uspto-grants-2010_02 |
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| ORD ID | ord-913790e8dc814b0eb10ee328dfdccae8 |
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| Source note | uspto-grants-2010_02 |
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