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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1925146Generated: October 26, 2026

Bromoacetyl bromide → N-(2-bromoacetyl)cyclopropanecarboxamide

https://huagongshe.com/reaction/1925146

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoacetyl bromideHCID 61147—
ReactantCyclopropanecarboxamideHCID 80376—
Solvent1,4-DioxaneHCID 31275—
ProductN-(2-bromoacetyl)cyclopropanecarboxamideHCID 5923301397.1%

Reaction Conditions

Temperature60 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178534B2
Source datasetuspto-grants-2012_05
ORD IDord-30325aeabe6e4fcf8b30181cab4b9529
Source noteuspto-grants-2012_05