HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1848505Generated: November 3, 2026
Trifluoroacetic acid → HCID 86709515, compound
https://huagongshe.com/reaction/1848505
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Di-tert-butyl dicarbonate | HCID 90495 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 86709514 | HCID 86709514 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86709515 | HCID 86709515 | — |
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. LC/MS: [(M+1)]+=285
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08952166B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-392fdf9ebd6e47998f697253f37529b6 |
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| Source note | uspto-grants-2015_02 |
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