HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 55665Generated: October 23, 2026
Decanoyl chloride → Decanoic acid 1,1-diethyl-3-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]propyl ester hydrochloride
https://huagongshe.com/en/reaction/55665
Participants
| Role | Name | HCID | Charge |
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| Reactant | Decanoyl chloride | HCID 66982 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 6-Fluoro-3-[1-(3-hydroxy-3-ethylpentyl)4-piperidinyl]-1,2-benzisoxazole | HCID 18467342 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Decanoic acid 1,1-diethyl-3-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]propyl ester hydrochloride | HCID 86749760 | 81% |
Reaction Steps
To a solution of 6-fluoro-3-[1-(3-hydroxy-3-ethylpentyl)-4-piperidinyl]-1,2-benzisoxazole (2.5 g, 7.48 mmol) in DCM (100 ml) was added decanoyl chloride (1.5 ml, 7.48 mmol) at 0 C., under nitrogen. The reaction mixture was stirred for 4 days at which time it was poured into NaHCO3 (sat., 50 ml). The layers were separated and the aqueous phase was extracted with DCM (2×). The combined organics were dried, filtered and concentrated to give the crude product which was purified via flash column chromatography (silica gel, 20-40% EtOAc/DCM). The product containing fractions were concentrated to give 3.0 g (81%) of the desired product as a yellow oil. The hydrochloride salt was prepared in anhydrous ether (60 ml) and isopropanol (1 ml) with ethereal HCl. The white salt was filtered and washed with anhydrous ether, m.p.=159°-161° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05624927 |
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| Source dataset | uspto-grants-1997_04 |
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| ORD ID | ord-8e459de1b6a740b9b4d53a7d478c98d5 |
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| Source note | uspto-grants-1997_04 |
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