HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1493272Generated: October 25, 2026
1-(2-Methoxyphenyl)piperazine → o-(1-Piperazinyl)phenol dihydrobromide
https://huagongshe.com/reaction/1493272
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-(2-Methoxyphenyl)piperazine | HCID 1346 | — |
| Reactant | p-(1-Piperazinyl)phenol dihydrobromide | HCID 2723591 | — |
| Reactant | Piperazine dihydrobromide | HCID 3017157 | — |
| Product | o-(1-Piperazinyl)phenol dihydrobromide | HCID 3017100 | — |
Reaction Steps
4-(=- 1)piperazine dihydrobromide may be prepared in the following manner: the experiment is carried out as in Example 8 for the preparation of 4-(4hydroxyphenyl)piperazine dihydrobromide, starting with 4-(2-methoxypheny)piperazine (25 g) and 47% aqueous solution of hydrdromic acid (360 cc). The mixture is heated at boiling point for 9 hours, the cooled to a temperature close to 20° C. Stirring is maintained for 15 hours at this temperature, then the mixture is concentrated at 40° C underreduced pressure (20 mm g; 2.7 kPa). The residual oil is redissolved in acetonitrile (40 cc) and isopropyl oxide (40 cc); the precipitate formed is separated by filtration, washed with oxide (2×50 cc). 4-(2-Hydroxyphenyl)piperazine dihydrobromide (m.p.: 235° C.) (18g) is obtained, which is used in the crude state in the subsequent syntheses.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05021420 |
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| Source dataset | uspto-grants-1991_06 |
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| ORD ID | ord-5bb11109698744f8b57df7930ade6bb4 |
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| Source note | uspto-grants-1991_06 |
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