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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1038536Generated: October 31, 2026

Bromoacetyl bromide → HCID 86647191, compound

https://huagongshe.com/reaction/1038536

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoacetyl bromideHCID 61147—
Reactant(Z)-1-{4-[2-(benzyloxy)-1,1,1,3,3,3-hexafluoropropan-2-yl]-2-(prop-1-en-1-yl)phenyl}piperazineHCID 86647190—
SolventDichloromethaneHCID 6344—
ProductHCID 86647191HCID 8664719147%

Reaction Steps

(Z)-1-{4-[2-(benzyloxy)-1,1,1,3,3,3-hexafluoropropan-2-yl]-2-(prop-1-en-1-yl)phenyl}piperazine (38 mg, 0.0595 mmol) was dissolved in dichloromethane (1.0 mL). Under ice-cold conditions, N,N′-dimethylaniline (9.0 μL, 0.0714 mmol) and bromoacetylbromide (5.5 μL, 0.0625 mmol) were added, and the mixture was stirred under ice-cold conditions for 0.5 hours. Then, under ice-cold conditions, N,N′-dimethylaniline (9.0 μL, 0.0714 mmol) and bromoacetylbromide (5.5 μL, 0.0625 mmol) were added, and the mixture was stirred under ice-cold conditions for 0.5 hours. The reaction solution was concentrated in vacuo, and the obtained residue was purified by silica-gel column chromatography (hexane/acetone). The title compound (16 mg (yield 47%)) was obtained as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08551985B2
Source datasetuspto-grants-2013_10
ORD IDord-d24531caa7e44d06821cdf36f61389ea
Source noteuspto-grants-2013_10