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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1248507Generated: November 3, 2026

Acetic Acid → HCID 12694032, compound

https://huagongshe.com/reaction/1248507

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantBenzyl mercaptanHCID 7509—
ReactantBoron trifluoride etherateHCID 8000—
ReactantHCID 12694024HCID 12694024—
ProductHCID 12694032HCID 12694032—

Reaction Conditions

Temperature65 °C

Reaction Steps

A mixture of 4-(2,5-difluorophenyl)-4-hydroxy-1-methyl-piperidine, free base of a, 4 ml of boron trifluoride etherate, 5 ml of benzyl mercaptan and 5 ml of glacial acetic acid is stirred at 65° C. for 16 hours. Excess acid is removed under reduced pressure with the residue equilibrated with 0.5N hydrochloric acid and ether and the resulting solution is stirred at 10°-20° C. for four hours. The resulting crystalline precipitate is sequentially collected by filtration, basified and extracted with ether providing the desired product as an oil. The oil is converted to its maleic acid salt which is recrystallized from an acetone-ether mixture to provide prisms, m.p. 164°-166° C. of 4-benzylthio-4-(2,5-difluorophenyl)-1-methylpiperidine maleate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04524207
Source datasetuspto-grants-1985_06
ORD IDord-c9bf17fc245244adaf5d80ddab34ecff
Source noteuspto-grants-1985_06