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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1079389Generated: November 1, 2026

Trifluoroacetic acid → HCID 53864130, compound

https://huagongshe.com/reaction/1079389

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 23366953HCID 23366953—
ProductHCID 53864130HCID 53864130142.7%

Reaction Steps

To 1-tert-Butyloxycarbonyl-4-[(4-dimethylaminophenyloxy)methyl]piperidine (0.1 g) obtained in Example 13 was added trifluoroacetic acid (0.5 ml) followed by stirring at room temperature for 10 minutes. The reaction mixture was concentrated under reduced pressure, and the concentrate was diluted with methylene chloride (100 ml) and washed with aqueous saturated solution of sodium bicarbonate. The organic layer was separated, dried over sodium sulfate and concentrated under reduced pressure. The residue was treated with fumaric acid and the resulting fumarate was recrystallized from methanol to obtain 4-[(4-dimethylaminophenyloxy)methyl]piperidine 1/2 fumarate (0.1 g) as pale yellow crystals, m.p. 210°-213° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05580883
Source datasetuspto-grants-1996_12
ORD IDord-b35a066468e2454eae31ef296f8b4c30
Source noteuspto-grants-1996_12