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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 508392Erstellt: 24. Oktober 2026

Ethanolamine → ethyl N-(2-hydroxyethyl)carbamate

https://huagongshe.com/de/reaction/508392

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolamineHCID 700—
EduktEthyl chloroformateHCID 10928—
EduktN-HydroxysuccinimideHCID 80170—
EduktDiisopropylethylamineHCID 81531—
LösungsmittelDichloromethaneHCID 6344—
Produktethyl N-(2-hydroxyethyl)carbamateHCID 223805—

Reaktionsschritte

To a stirred solution of ethyl chloroformate (4 g, 0.037 mol.) and N-hydroxysuccinimide (6.3 g, 0.055 mol.) in 10 mL of DCM at 0° C. under nitrogen atmosphere was added N,N-Diisopropylethylamine (9.5 g, 0.055 mol) in 10 mL of DCM. The progress of the reaction was monitored by thin layer chromatography (TLC). After stirring for 3 hrs at room temperature, the reaction mixture was filtered and the precipitate was washed with 2×10 mL of dichloromethane. The combined filtrate was evaporated and dissolved in 20 mL of acetonitrile, cooled in an ice-bath and then added dropwise a solution of Ethanolamine 23 (3.3 mL, 2.5 eq). The resulting mixture was stirred at ice-bath temperature for 1 h and then overnight at room temperature. The progress of the reaction was monitored by thin layer chromatography (TLC). The reaction mixture was filtered, and the precipitate was washed with 2×10 mL DCM and dried over sodium sulfate. After removing the solvent under reduced pressure, the residue was purified by silica gel column chromatography to give ethyl (2-hydroxyethyl)carbamate.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09096515B2
Quelldatensatzuspto-grants-2015_08
ORD IDord-452b771435f541efa7498b17b2532eee
Quellennotizuspto-grants-2015_08