HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 342553Generated: October 30, 2026
Hydrogen Bromide → 1-[2-(2,2,2-Trifluoroethoxy)-4-hydroxyphenyl]piperazine hydrobromide
https://huagongshe.com/reaction/342553
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | 1-[2-(2,2,2-Trifluoroethoxy)-4-methoxyphenyl]piperazine | HCID 70198216 | — |
| Product | 1-[2-(2,2,2-Trifluoroethoxy)-4-hydroxyphenyl]piperazine hydrobromide | HCID 70204241 | — |
Reaction Steps
A mixture of 1-[2-(2,2,2-trifluoroethoxy)-4-methoxyphenyl]piperazine (1.87 g, 6.4 mmol) and 48% aqueous hydrobromic acid (5 mL) was heated 17 hours at reflux. The reaction mixture was allowed lo cool and then concentrated in vacuo. The residue was dissolved in ethanol (10 mL) at approximately 55° C. and the solution was cooled to 0° C. The solids were collected, washed with cold ethanol (3×10 mL) and dried in vacuo at approximately 80° C. to give 1-[2-(2,2,2-trifluoroethoxy)-4-hydroxyphenyl]piperazine hydrobromide, m.p. 190-194. Anal.: Calcd. for C12H14F3N2O2.(HBr)0.5. H2O: C, 43.00; H, 5.27; N, 8.37%; Found: C, 43.41; H, 4.97; N, 8.36%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05859014 |
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| Source dataset | uspto-grants-1999_01 |
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| ORD ID | ord-8ddf585c0cb04f638be63fa2f83b5897 |
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| Source note | uspto-grants-1999_01 |
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