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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 411270Generated: October 30, 2026

Trifluoroacetic acid → HCID 9861312, compound

https://huagongshe.com/reaction/411270

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
ReactantSodium BicarbonateHCID 516892—
Reactanttert-Butyl 4-(methylamino)piperidine-1-carboxylateHCID 15380702—
ReactantHCID 22048569HCID 22048569—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductHCID 9861312HCID 986131282.8%

Reaction Steps

A solution of 1.86 g of 2-[4-(tert-butoxycarbonylamino)-2,3,5-trimethylphenoxy]acetic acid, 1.43 g of 1-(tert-butoxycarbonyl)-4-methylaminopiperidine, 2.94 g of benzotriazol-1-yloxytris(dimethylamino)phosphonium hexafluorophosphate (BOP Reagent) and 1.26 ml of triethylamine in 30 ml of dimethylformamide was stirred over night at room temperature. Then, 15 ml of saturated sodium hydrogen carbonate solution was added to the reaction mixture and the mixture was extracted with ethyl acetate. The extract was washed with brine, dried and concentrated under reduced pressure to give a residue. The obtained residue was dissolved in 30 ml of methylene chloride, and to this solution was added 7.5 ml of trifluoroacetic acid at 0° C., then the mixture was stirred for 2 hours at room temperature. After removal of the solvent, the resultant residue was purified by silica gel column chromatography (methylene chloride:methanol=12:1) to give 1.52 g (81%) of the above-mentioned compound (1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06559146B1
Source datasetuspto-grants-2003_05
ORD IDord-f70f1ae023424d6aba6c3bd4f958eea2
Source noteuspto-grants-2003_05