HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2184564Generated: October 31, 2026
Potassium Carbonate → 3-Hydroxybutyl 4-methylbenzenesulfonate
https://huagongshe.com/reaction/2184564
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | p-Toluenesulfonate | HCID 85570 | — |
| Reactant | 3-(4-Piperidyl)-6-fluoro-1,2-benzisoxazole | HCID 849421 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-Hydroxybutyl 4-methylbenzenesulfonate | HCID 13204323 | — |
Reaction Steps
Racemic 3-hydroxybutyl tosylate was prepared in a manner described by Ferreira et al., Tetrahedron, 46, pp. 6311-6318, (1990). To a solution of the racemic tosylate (9.2 g, 37.8 mmol) in acetonitrile (190 ml) was added 6-fluoro-3-(4-piperidinyl)-1,2-benzisoxazole (8.3 g, 37.7 mmol) followed by milled potassium carbonate (7.8 g. 56.6 mmol) at room temperature under nitrogen. The reaction mixture was warmed to reflux for 4.5 hours and allowed to cool to room temperature. The solids were removed via filtration through a pad of Celite and were washed with EtOAc. The combined filtrates were concentrated to give the crude product. Purification via preparative HPLC (silica gel, 10% MeOH/EtOAc) afforded 6.3 g (57%), m.p.=100°-101° C. ANALYSIS: Calculated for C16H21FN2O2: 65.73% C 7.24% H 9.58% N Found: 65.59% C 7.30% H 9.52% N
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | USRE037729E1 |
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| Source dataset | uspto-grants-2002_06 |
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| ORD ID | ord-0dcac2c37ea64121ac66ff845e0c3a82 |
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| Source note | uspto-grants-2002_06 |
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