HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 483353Generated: October 30, 2026
Hydrogen Bromide → HCID 19752458, compound
https://huagongshe.com/reaction/483353
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | 3'-Aminoacetophenone | HCID 7417 | — |
| Reactant | Ethyl Acrylate | HCID 8821 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Catalyst | HCID 178419072 | HCID 178419072 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 19752458 | HCID 19752458 | — |
Reaction Steps
solution of 5 g of m-aminoacetophenone in 100 ml of acetone was combined with 25 ml of water and 15 ml of 47% hydrobromic acid and the resultant mixture was stirred for 30 minutes with 10 ml of an aqueous solution containing 3.32 g of sodium nitrite added dropwise in advance thereto at 5 C. The produced reaction solution and 28 ml of ethyl acrylate added dropwise thereto and 0.53 g of copper (I) oxide added piecemeal thereto at 40° C. were stirred for 2 hours. The resultant mixture was combined with water, extracted with ethyl acetate An organic layer was washed with water and a saturated aqueous saline solution, dried with anhydrous magnesium sulfate, and distilled under a vacuum to expel the solvent to obtain ethyl 2-bromo-3-(3-acetylphenyl)propionate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05225426 |
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| Source dataset | uspto-grants-1993_07 |
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| ORD ID | ord-7b4f8c42917c4c74a0af40604cd5fc68 |
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| Source note | uspto-grants-1993_07 |
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