Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2284739Generated: October 30, 2026

Trifluoroacetic acid → HCID 90052146, compound

https://huagongshe.com/reaction/2284739

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 90052647HCID 90052647—
SolventDichloromethaneHCID 6344—
ProductHCID 90052146HCID 90052146—

Reaction Steps

To a solution of tert-butyl (4-(((benzyloxycarbonyl)amino)methyl)tetrahydro-2H-pyran-4-yl)carbamate (G16, 141 mg) in methylene chloride (2 mL), trifluoroacetic acid (2 mL) was added at room temperature, and the mixture was stirred at the same temperature for 1 hour. The solvent was evaporated under reduced pressure, and then ethyl acetate and saturated aqueous sodium hydrogencarbonate were added to the residue. The organic layer was separated, washed with saturated aqueous sodium chloride, and then dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure to obtain benzyl ((4-aminotetrahydro-2H-pyran-4-yl)methyl)carbamate (G17, 106 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145415B2
Source datasetuspto-grants-2015_09
ORD IDord-5f8684254c1c43b2a430e70500ed6cbd
Source noteuspto-grants-2015_09