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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 921670Generated: October 30, 2026

Trifluoroacetic acid → HCID 131732391, compound

https://huagongshe.com/reaction/921670

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 86708535HCID 86708535—
SolventDichloromethaneHCID 6344—
ProductHCID 131732391HCID 131732391140%

Reaction Steps

(3R,4S)-tert-butyl 3-fluoro-4-((methoxycarbonyl)amino)piperidine-1-carboxylate (127 mg, 0.460 mmol) was taken up in DCM (5 mL) and TFA (0.708 mL, 9.19 mmol) was added. The reaction was stirred at room temperature for 1 h. The solvent was removed in vacuo and the material was dissolved in MeOH. The solution was loaded onto an SCX column (5 g, benzenesulfonic acid sorbent) and the column was rinsed with MeOH, followed by 7N NH3/MeOH to obtain the product. The solvent was removed in vacuo to obtain methyl ((3R,4S)-3-fluoropiperidin-4-yl)carbamate (113.5 mg) as a colorless gum. The crude material was taken onto the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09273057B2
Source datasetuspto-grants-2016_03
ORD IDord-89e62dc5d9c040588ec2753d4f5ce986
Source noteuspto-grants-2016_03