HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 715923Generated: October 25, 2026
Hydrochloric Acid → 2,4-Dibromo-N-(4-bromophenyl)butanamide
https://huagongshe.com/reaction/715923
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-Bromoaniline | HCID 7807 | — |
| Reactant | 2,4-Dibromobutyryl chloride | HCID 4413143 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 2,4-Dibromo-N-(4-bromophenyl)butanamide | HCID 117874801 | — |
Reaction Steps
To a solution of 4-bromoaniline (1.73 g) in dichloromethane (40 ml), triethylamine (2.8 ml) and a solution of 2,4-dibromobutyryl chloride (3.2 g) in dichloromethane (10 ml) were added under ice cooling, and the mixture was stirred at room temperature for 5 hours. After addition of 1 N hydrochloric acid to the reaction solution, the mixture was separated into two layers. The aqueous layer was subjected to extraction with chloroform. The organic layers were combined, washed with a saturated aqueous solution of sodium bicarbonate and saturated saline in this order and then dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure to obtain a crude product of the title compound, which was used in the next reaction without being purified.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09187489B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-8338ee55c374481c9bb6df8e9bdb033b |
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| Source note | uspto-grants-2015_11 |
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