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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 235457Generated: October 26, 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/reaction/235457

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDecanoyl chlorideHCID 66982—
ReactantSodium BicarbonateHCID 516892—
Reactant6-Fluoro-3-[1-(3-hydroxy-3-ethylpentyl)4-piperidinyl]-1,2-benzisoxazoleHCID 18467342—
SolventDichloromethaneHCID 6344—
ProductDecanoic acid 1,1-diethyl-3-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]propyl ester hydrochlorideHCID 8674976081%

Reaction Steps

To a solution of 6-fluoro-3-[l-(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 (2X). 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05597842
Source datasetuspto-grants-1997_01
ORD IDord-4296c2d7ec714dbd88fa98258f5c4ed5
Source noteuspto-grants-1997_01