HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 647539Generated: October 29, 2026
Acetic Acid → 4-(2-Fluorobenzylthio)-4-(2-fluorophenyl)-1-methylpiperidine maleate
https://huagongshe.com/reaction/647539
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | 2-Fluorobenzyl mercaptan | HCID 522175 | — |
| Reactant | 4-(2-Fluorophenyl)-1-methylpiperidin-4-OL | HCID 12694023 | — |
| Product | 4-(2-Fluorobenzylthio)-4-(2-fluorophenyl)-1-methylpiperidine maleate | HCID 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 0.5 N 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 either, 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04409229 |
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| Source dataset | uspto-grants-1983_10 |
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| ORD ID | ord-7692d3272a46457999d2faf423027815 |
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| Source note | uspto-grants-1983_10 |
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