HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2358140Generated: October 25, 2026
Sulfuric Acid → Methyl 4-[2-fluoro-3-(methylsulfonyl)phenyl]piperazine-1-carboxylate
https://huagongshe.com/reaction/2358140
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Perhydroxyl radical | HCID 18500 | — |
| Reactant | Methyl 4-[2-fluoro-3-(methylthio)phenyl]piperazine-1-carboxylate | HCID 57448074 | — |
| Catalyst | Sodium tungstate | HCID 26052 | — |
| Product | Methyl 4-[2-fluoro-3-(methylsulfonyl)phenyl]piperazine-1-carboxylate | HCID 57448075 | — |
Reaction Steps
To an ice cooled solution of methyl 4-[2-fluoro-3-(methylthio)phenyl]piperazine-1-carboxylate (1.4 g, 4.9 mmol) in sulfuric acid (1 M, 10 ml) was added sodium tungstate (0.016 g, 0.05 mmol) in one portion followed by droppwise addition of hydroperoxide (30%, 1.25 ml, 12.2 mmol). The reaction mixture was warmed to 55° C. and was stirred for 20 h. The reaction mixture was brought to ambient temperature and aqueous sodium hydroxide (5 M, 50 ml) was added. The aqueous phase was extracted with ethyl acetate (2×50 ml). The combined organic phase was dried (MgSO4) and evaporated to dryness to give the title compound. Yield (1.1 g). MS m/z (rel. intensity, 70 eV) 316 (M+, 58), 296 (30), 228 (bp), 216 (38), 56 (71).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07763639B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-9c460f7b015a4477bbab89834c3f88e9 |
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| Source note | uspto-grants-2010_07 |
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