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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1501818Generated: November 4, 2026

Trifluoroacetic acid → HCID 86709515, compound

https://huagongshe.com/reaction/1501818

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantPotassium CarbonateHCID 11430—
ReactantDi-tert-butyl dicarbonateHCID 90495—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 86709514HCID 86709514—
SolventDichloromethaneHCID 6344—
ProductHCID 86709515HCID 86709515—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 1-tert-butyl 4-methyl 4-(2-((tert-butoxycarbonyl)amino)-1-hydroxypropyl)piperidine-1,4-dicarboxylate (8000 mg, 19.2 mmol) in DCM (190 mL) was added TFA (44.4 mL, 576 mmol) at 0° C. and the resulting solution was stirred for 2 h. After removing the volatiles, high vacuum was applied briefly to remove excess TFA, and the residue was dissolved in MeOH (190 mL), and K2CO3 (26.5 g, 192 mmol) was added. The reaction mixture was heated at 60° C. for 2 h. After cooling to room temperature, saturated NaHCO3 solution (60 mL) was added, followed by (BOC)2O (12.6 g, 57.6 mmol). The reaction mixture was stirred overnight, and extracted with DCM. The organic layer was dried with MgSO4, and concentrated to give the crude product, which was purified by column chromatography (0-20% MeOH/DCM, monitored at 210 nM) to give the title compound. LCMS: [(M+1)]+=285

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206198B2
Source datasetuspto-grants-2015_12
ORD IDord-4c3f0913e9d046bab1325b6104a89b97
Source noteuspto-grants-2015_12