HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1925146Generated: October 26, 2026
Bromoacetyl bromide → N-(2-bromoacetyl)cyclopropanecarboxamide
https://huagongshe.com/reaction/1925146
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromoacetyl bromide | HCID 61147 | — |
| Reactant | Cyclopropanecarboxamide | HCID 80376 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | N-(2-bromoacetyl)cyclopropanecarboxamide | HCID 59233013 | 97.1% |
Reaction Steps
Cyclopropanecarboxamide (58.7 g, 690 mmol) in 1,4-Dioxane (1600 ml) was added 2-bromoacetyl bromide (59.9 ml, 690 mmol) at room temperature and stirred for 4 h at 60° C. The reaction mixture was concentrated to dryness. The residue was dissolved in EtOAc and carefully washed with satd. NaHCO3, water then with brine solution, dried over Na2SO4 and concentrated to get N-(2-bromoacetyl)cyclopropanecarboxamide (138 g, 670 mmol, 97% yield) as an off white solid. This material was used without purification. ESI-MS:m/z 208.0 (M+2H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08178534B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-30325aeabe6e4fcf8b30181cab4b9529 |
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| Source note | uspto-grants-2012_05 |
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