HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2394549Generated: October 28, 2026
Sodium Bicarbonate → HCID 10454460, compound
https://huagongshe.com/reaction/2394549
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3-(4-Piperidyl)-6-fluoro-1,2-benzisoxazole | HCID 849421 | — |
| Reactant | 4-(3-Chloropropoxy)-3-hydroxy-alpha-methylbenzenemethanol | HCID 10398986 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 10454460 | HCID 10454460 | 106.4% |
Reaction Steps
A mixture of 6-fluoro-3-(4-piperidinyl)-1,2-benzisoxazole (4.3 g, 19.5 mmol), 4-(3-chloropropoxy)-3-hydroxy-α-methylbenzenemethanol (4.5 g, 19.5 mmol), KI (200 mg), NaHCO3 (1.8 g, 21.5 mmol) and CH3CN (125 ml) was stirred at reflux under nitrogen for 24 hours. The cooled reaction was filtered and the filter cake was washed with CH3CN. The filtrate was concentrated to afford an oily residue, which was partitioned between water and ethyl acetate. The ethyl acetate extract was washed with water, dried with MgSO4, and concentrated to yield 8.6 g of a dark oil. The oil was purified by preparative HPLC (Waters Associates prep LC/system 500) to yield 5.0 g. The compound was recrystallized twice from ethanol to provide 3.9 g (49%) of 4-[3-4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]-propoxy]-3-hydroxy-α-methyl-benzene methanol as a light beige solid, m.p.=142°-144° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05811430 |
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| Source dataset | uspto-grants-1998_09 |
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| ORD ID | ord-e1bcbaf00fca4de983ae9f0ae28d5785 |
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| Source note | uspto-grants-1998_09 |
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