HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 458804Generated: October 29, 2026
Bromoacetyl bromide → HCID 18442580, compound
https://huagongshe.com/reaction/458804
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bromoacetyl bromide | HCID 61147 | — |
| Reactant | HCID 18442568 | HCID 18442568 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 18442580 | HCID 18442580 | 70.1% |
Reaction Steps
1-(2-Amino-4,5-dimethoxy-phenyl)-2-(3,4-dichloro-phenyl)-ethanone (5.52 g, 16.24 mmol) was dissolved in dichloromethane (20 ml), distilled water was then added (2 ml) and the resulting solution was cooled at −5° C. under nitrogen. Bromoacetylbromide (1.63 ml, 18.68 mmol) was dissolved in dichloromethane (10 ml) and added dropwise to the previous solution; the temperature was not allowed to exceed +5° C. The reaction mixture was stirred at 0° C. for 15 min and then allowed to reach the RT before further stirring for 2.5 h. Dichloromethane was added (30 ml) and the organic layer was washed with distilled water, saturated NaHCO3 solution, and brine. It was dried over magnesium sulfate, filtered and the solvent was removed under vacuum. This crude mixture was purified by flash chromatography (dichloromethane/methanol, 360/1) to give the product as a yellow solid (5.25 g, 70%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07192950B2 |
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| Source dataset | uspto-grants-2007_03 |
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| ORD ID | ord-5da54e4f22054c43afc4f3c7f4c9049b |
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| Source note | uspto-grants-2007_03 |
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