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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 510193Generated: October 31, 2026

1,2-Dichloroethane → N2-(tert-butoxycarbonyl)-3-hydroxy-N-(2,2,2-trifluoroethyl)-D-valinamide

https://huagongshe.com/reaction/510193

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant2,2,2-Trifluoroethylamine hydrochlorideHCID 9772—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
ReactantN-(tert-Butoxycarbonyl)-3-hydroxy-D-valineHCID 11299247—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductN2-(tert-butoxycarbonyl)-3-hydroxy-N-(2,2,2-trifluoroethyl)-D-valinamideHCID 89495520—

Reaction Steps

To a vial was added (R)—N-Boc-2-amino-3-hydroxy-3-methylbutanoic acid (CA, 500 mg, 2.144 mmol), 2,2,2-trifluoroethanamine hydrochloride (581 mg, 4.29 mmol), EDC (493 mg, 2.57 mmol), and HOBT (328 mg, 2.144 mmol). The reactants were dissolved in DCM (10 mL) and then DIEA (1.497 mL, 8.57 mmol) was added. The mixture was allowed to stir at RT overnight. The mixture was diluted with ethyl acetate, washed 2× with aqueous sodium hydrogen carbonate and 1× with brine. Aqueous layers were back extracted once with ethyl acetate, combined organic layers were dried with Na2SO4, filtered and the solvent was evaporated under reduced pressure. The material I-27a was used directly in the subsequent step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096598B2
Source datasetuspto-grants-2015_08
ORD IDord-fdc15f59045d4c0b85560e8fb6b3ce9e
Source noteuspto-grants-2015_08