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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1248512Generated: November 1, 2026

Acetic Acid → 4-(2-Fluorobenzylthio)-4-(2-fluorophenyl)-1-methylpiperidine maleate

https://huagongshe.com/reaction/1248512

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantBoron trifluoride etherateHCID 8000—
Reactant(2-Fluorophenyl)methanethiolHCID 522175—
Reactant4-(2-Fluorophenyl)-1-methylpiperidin-4-OLHCID 12694023—
Product4-(2-Fluorobenzylthio)-4-(2-fluorophenyl)-1-methylpiperidine maleateHCID 12694040—

Reaction Steps

A mixture of 4-(2-fluorophenyl)-4-hydroxy-1-methylpiperidine of Example 1a (15.8 g), 12 ml of 2-fluorobenzyl mercaptan and 20 ml of boron trifluoride etherate in 15 ml of glacial acetic acid is stirred at 65°-70° C. for 16 hours. The excess reagents are removed under reduced pressure, the residue is triturated with 300 ml of 0.5N HCl and 100 ml of ether. After standing at 5°-10° C. for 30 minutes, a crystalline precipitate is filtered, air dried and made basic with 10% aqueous NH4OH. The liberated amine is taken up in ether, dried and concentrated to a yellowish oil which is then converted to its maleate in ether, recrystallization of the crude salt from methanol-ether gives colorless prisms, m.p. 153°-154° C. of 4-(2-fluorobenzylthio)-4-(2-fluorophenyl)-1-methylpiperidine maleate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04524207
Source datasetuspto-grants-1985_06
ORD IDord-3e3c249d726546f1be4b4dc3421cc9a2
Source noteuspto-grants-1985_06