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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 242403Generated: October 31, 2026

Ethanamine, 2,2,2-trifluoro- → Tert-butyl (2-oxo-2-((2,2,2-trifluoroethyl)amino)ethyl)carbamate

https://huagongshe.com/reaction/242403

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanamine, 2,2,2-trifluoro-HCID 9773—
ReactantN-(tert-butoxycarbonyl)glycineHCID 78288—
ReactantDiisopropylethylamineHCID 81531—
ReactantPyBOPHCID 2724699—
SolventDichloromethaneHCID 6344—
ProductTert-butyl (2-oxo-2-((2,2,2-trifluoroethyl)amino)ethyl)carbamateHCID 71623152—

Reaction Steps

DIPEA (15 ml) is added to a solution of N-(tert-butoxycarbonyl)glycine (5.0 g), PYBOP (benzotriazol-1-yl-oxytripyrrolidinophosphonium hexafluorophosphate, 16.3 g) and 2,2,2-trifluorethylamine (2.47 ml) in dichloromethane (48 ml). After 24 hours at room temperature, the reaction is quenched with water and extracted three times with dichloromethane. The combined organic phases are washed with HCl (2M), Na2CO3 (1M) and a saturated aqueous solution of NaCl, dried over MgSO4 and concentrated in vacuo. The crude product is purified by column chromatography (450 g) eluting with a mixture of ethyl acetate and hexane (2:3 to 3:2) to yield [(2,2,2-trifluoro-ethylcarbamoyl)-methyl]-carbamic acid tert-butyl ester (3.89 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653116B2
Source datasetuspto-grants-2014_02
ORD IDord-d532443417c2454fbe701d226f1fec14
Source noteuspto-grants-2014_02