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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1018937Generated: October 30, 2026

4-Fluorobenzyl chloride → HCID 9797495, compound

https://huagongshe.com/reaction/1018937

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Fluorobenzyl chlorideHCID 9602—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(2,3-Dihydro-benzo[1,4]dioxin-6-yl)-piperazineHCID 1071338—
ReactantHCID 18399633HCID 18399633—
SolventAcetonitrileHCID 6342—
ProductHCID 9797495HCID 979749534%

Reaction Steps

A solution of 1-(1,4-benzodioxan-6-yl)piperazine prepared as described in Example 1 (0.146 g, 0.663 mmol) in CH3CN (5 mL) is treated with potassium carbonate (0.458 g, 3.32 mmol) and 4-fluorobenzyl chloride (0.144 g, 0.995 mmol). The mixture is heated at reflux for 4 hours. The resulting mixture is then cooled to room temperature and washed successively with saturated aqueous NH4Cl (20 mL) and saturated aqueous NaCl (20 mL). The organic portion is dried over Mg2SO4, filtered and concentrated. Purification by flash column chromatography (30% ethyl acetate-hexane) gives 0.074 g (34%) of 1-(1,4 benzodioxan-6-yl)-4-(4-fluorobenzyl)piperazine as a white solid (TLC Rf 0.35; 30% ethyl acetate:hexane). A solution of this material in 1 mL of ethanol is treated with oxalic acid (0.020 g, 0.225 mmol) and concentrated to give 1-(1-(1,4-benzodioxan-6-yl)-4-(4-fluorobenzyl)piperazine oxalic acid salt (Compound 1) 0.079 g (88%), m.p. 177-179° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06486164B2
Source datasetuspto-grants-2002_11
ORD IDord-a7a6ab4e7b734864b4d8bca1c1c3b30b
Source noteuspto-grants-2002_11