HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1641469Generated: November 1, 2026
Hydrochloric Acid → 2-amino-3-bromo-5-chloro-N-(1-cyclopropylethyl)benzamide
https://huagongshe.com/reaction/1641469
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-amino-5-chloro-N-(1-cyclopropylethyl)benzamide | HCID 43533096 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-amino-3-bromo-5-chloro-N-(1-cyclopropylethyl)benzamide | HCID 66736289 | — |
Reaction Steps
0.1 g of 2-amino-5-chloro-N-(1-cyclopropylethyl)benzamide was dissolved in 3 ml of N,N-dimethylformamide and cooled to 0° C. 0.02 g of sodium hydride was added, followed by stirring for one hour, and 0.09 g of bromine was added, followed by stirring for 2 hours. The reaction liquid was added to a 1 M-HCl aqueous solution, followed by extraction with ethyl acetate. The organic layer was washed with a saturated sodium chloride aqueous solution and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=1/0 to 1/1) to obtain 0.08 g of the pale yellow desired produce (melting point: 177° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08115006B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-0a0ec19efa3148e4b8d1e758e586ac3d |
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| Source note | uspto-grants-2012_02 |
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