HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1674988Generated: November 1, 2026
4-Hydroxybenzoic Acid → HCID 28798584, compound
https://huagongshe.com/reaction/1674988
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Hydroxybenzoic Acid | HCID 135 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | HCID 67340847 | HCID 67340847 | — |
| Solvent | Hydrogen Bromide | HCID 260 | — |
| Product | HCID 28798584 | HCID 28798584 | 95.3% |
Reaction Steps
(R)-1-(1-(4-Bromophenyl)ethyl)-4-tosylpiperazine (4.44 g, 10.49 mmol) and 4-hydroxybenzoic acid (4.35 g, 31.46 mmol) in hydrobromic acid (33% in AcOH, 40 mL,) were stirred at room temperature for 48 hours. Water (40 mL) was then added to the dark mixture and stirring continued for a further 2 hours to give a beige solid, which was filtered off and washed with water (10 mL). The combined filtrate and washings were washed with toluene (3×50 mL) then cooled to 5° C. and basified to pH>10 with 40% NaOH. The resulting mixture was extracted with tert butyl methyl ether (2×50 mL) and the combined extracts washed with saturated brine, dried over MgSO4 and evaporated to give (R)-1-[1-(4-bromophenyl)ethyl]piperazine (2.69 g, 95%) as an orange, viscous oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08003649B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-55de1ef5ce1946b18237d68991d13e76 |
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| Source note | uspto-grants-2011_08 |
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