HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1018937Generated: October 30, 2026
4-Fluorobenzyl chloride → HCID 9797495, compound
https://huagongshe.com/reaction/1018937
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Fluorobenzyl chloride | HCID 9602 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(2,3-Dihydro-benzo[1,4]dioxin-6-yl)-piperazine | HCID 1071338 | — |
| Reactant | HCID 18399633 | HCID 18399633 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 9797495 | HCID 9797495 | 34% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06486164B2 |
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| Source dataset | uspto-grants-2002_11 |
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| ORD ID | ord-a7a6ab4e7b734864b4d8bca1c1c3b30b |
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| Source note | uspto-grants-2002_11 |
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