HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1280725Generated: November 2, 2026
HCID 9924295, compound → HCID 69969745, compound
https://huagongshe.com/reaction/1280725
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 9924295 | HCID 9924295 | — |
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 69969745 | HCID 69969745 | 10.2% |
Reaction Steps
(2RS,3R)-4-[1-(2-Fluoro-4-phenyl-butyl)-pyrrolidin-3-ylsulfanyl]-phenol (0.56 g, 1.62 mmol) was dissolved in MeOH (50 ml), cooled to 0° C. and treated with oxone (0.5 g, 0.81 mmol). After 4 hours stirring at 0° C., reaction mixture was quenched with saturated NaHCO3 (65 ml). Aqueous phase was extracted with CH2Cl2 (6 times). Combined organic phases were dried over Na2SO4 and the solvent was evaporated. The residue was chromatographed by MPLC over silica gel (CH2Cl2—MeOH, 99:1 then 98:2) then by preparative HPLC (EtOH-heptane, 08:92, detection at 254 nm) to provide (2R,3R, S-oxide R)-4-[1-(2-fluoro-4-phenyl-butyl)-pyrrolidine-3-sulfinyl]-phenol (30 mg, first fraction, 5%), MS: m/e=362.2 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06451819B2 |
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| Source dataset | uspto-grants-2002_09 |
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| ORD ID | ord-b95285b7f9f449efb71a3b5ce80a85ac |
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| Source note | uspto-grants-2002_09 |
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