HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1009463Generated: October 30, 2026
Water → 2-Bromo-N-(4-methoxybenzyl)acetamide
https://huagongshe.com/reaction/1009463
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Bromoacetyl bromide | HCID 61147 | — |
| Reactant | 4-Methoxybenzylamine | HCID 75452 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Bromo-N-(4-methoxybenzyl)acetamide | HCID 46736691 | 43.8% |
Reaction Steps
7.42 g of 4-methoxybenzylamine was dissolved in 70 mL of methylene chloride, and a solution (10 mL) of 23.2 g of bromoacetyl bromide in methylene chloride was added thereto at −10° C. To the reaction liquid was added dropwise a solution (10 mL) of 8.0 mL of triethylamine in methylene chloride at 0° C., followed by stirring at room temperature for 30 minutes. To the reaction liquid was added water under ice-cooling, followed by extraction with methylene chloride. The organic layer was washed with an aqueous saturated sodium hydrogen carbonate solution, and then dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the obtained residue was purified by silica gel column chromatography (hexane:ethyl acetate=90:10 to 0:100) to obtain a product, which was recrystallized from ethyl acetate to obtain 6.11 g of 2-bromo-N-(4-methoxybenzyl)acetamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07973078B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-1560ad2b7e8c45cda84cbee322211730 |
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| Source note | uspto-grants-2011_07 |
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