Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814742Generated: October 31, 2026

Bromoacetyl bromide → HCID 22498793, compound

https://huagongshe.com/reaction/1814742

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoacetyl bromideHCID 61147—
ReactantHCID 22498786HCID 22498786—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22498793HCID 2249879337.3%

Reaction Steps

To a stirred solution of the above 2-(2,2-dimethyl-propylamino)-1-morpholin-4-yl-ethanone (0.18 g, 0.8 mmol) in THF (2.0 mL), a solution of bromoacetyl bromide (0.15 mL, 1.6mmol) in THF (2.0 mL) was added, dropwise at −78° C., under nitrogen. After 3 h the reaction was concentrated and the resulting residue was diluted with methylene chloride and saturated NaHCO3. The layers were separated and the aqueous phase was extracted with methylene chloride. The combined organic layers were dried (MgSO4), filtered and concentrated to give the crude product. Purification via silica gel flash chromatography, eluting with EtOAc, flow rate 30 mL/min, gave 0.10 g (36%) of 2-bromo-N-(2,2-dimethyl-propyl)-N-(2-morpholin-4-yl-2-oxo-ethyl)-acetamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06878706B1
Source datasetuspto-grants-2005_04
ORD IDord-aabbb1a2e9a64901af9c71489917fa77
Source noteuspto-grants-2005_04