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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1254336Generated: November 3, 2026

1,2-Dichloroethane → HCID 59382986, compound

https://huagongshe.com/reaction/1254336

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant4-MethylmorpholineHCID 7972—
ReactantEthanamine, 2,2,2-trifluoro-HCID 9773—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant(2S)-2-(((tert-butoxy)carbonyl)amino)-3-cyclohexylpropanoic acidHCID 10588189—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 59382986HCID 5938298680%

Reaction Steps

A mixture of (2S)-2-tert-butoxycarbonylamino-3-cyclohexyl-propionic acid (2.98 g, 11 mmol), 2,2,2-trifluoroethylamine (1.35 g, 10 mmol), EDC (2.87 g, 15 mmol), HOBt (2.03 g, 15 mmol) and NMM (5.05 g, 50 mmol) in 100 mL of CH2Cl2 was stirred overnight. The mixture was poured into water (50 mL) and extracted with CH2Cl2 (3×50 mL). The combined organic extracts were washed with brine (50 mL), dried over Na2SO4, and evaporated to give the residue. The residue was purified by silica chromatography to give tert-butyl (S)-1-(2,2,2-trifluoroethylcarbamoyl)-2-cyclohexylethylcarbamate (2.8 g, 80%). 1H NMR (CDCl3, 400 MHZ) δ 0.90 (m, 2 H), 1.25 (m, 4 H), 1.44 (s, 9 H), 1.68 (m, 7 H), 3.89 (m, 1 H), 4.16 (brs, 1 H), 4.82 (brs, 1 H), 6.78 (brs, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455521B2
Source datasetuspto-grants-2013_06
ORD IDord-40e663a39b88480bb479b031f55a1864
Source noteuspto-grants-2013_06