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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1768571Generated: October 25, 2026

Water → 3-[1-(1-Hydroxyhex-6-yl]-4-piperidinyl]-6-fluoro-1,2-benzisoxazole

https://huagongshe.com/reaction/1768571

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantLithium CarbonateHCID 11125—
Reactant6-Chloro-1-hexanolHCID 74828—
ReactantR-56109 hydrochlorideHCID 11334359—
SolventDimethylformamideHCID 6228—
Product3-[1-(1-Hydroxyhex-6-yl]-4-piperidinyl]-6-fluoro-1,2-benzisoxazoleHCID 1894893025.6%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 6-fluoro-3-(4-piperidinyl)-1,2-benzisoxazole hydrochloride (1g, 3.9 mmol), lithium carbonate (865 mg, 1.7 mmol) and 6-chloro-1-hexanol (534 mg, 3.9 mmol) in 5 ml dry DMF was heated at 100° C. for 48 h. The reaction was poured into water and the aqueous mixture was extracted with ethyl acetate. The ethyl acetate phase was washed with water, brine, dried with sodium sulphate and concentrated in vacuo. The crude product was purified by chromatography on silica gel 60 eluting with ethyl acetate:methanol (9:1, v/v). Concentration of the appropriate fractions afforded 310 mg (25.6%) of 3-[1-(1-hydroxyhex-6-yl)-4-piperidinyl]-6-fluoro-1, 2-benzisoxazole as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05378714
Source datasetuspto-grants-1995_01
ORD IDord-e842eb7785cb422790b5f8f18349cf51
Source noteuspto-grants-1995_01