HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1038536Generated: October 31, 2026
Bromoacetyl bromide → HCID 86647191, compound
https://huagongshe.com/reaction/1038536
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromoacetyl bromide | HCID 61147 | — |
| Reactant | (Z)-1-{4-[2-(benzyloxy)-1,1,1,3,3,3-hexafluoropropan-2-yl]-2-(prop-1-en-1-yl)phenyl}piperazine | HCID 86647190 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86647191 | HCID 86647191 | 47% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08551985B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-d24531caa7e44d06821cdf36f61389ea |
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| Source note | uspto-grants-2013_10 |
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