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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 891738Erstellt: 25. Oktober 2026

Toluene → tert-Butyl (2-azidoethyl)carbamate

https://huagongshe.com/reaction/891738

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTolueneHCID 1140—
EduktTriphenylphosphineHCID 11776—
EduktP,P-Diphenylphosphinic azideHCID 199401—
Edukttert-butyl N-(2-hydroxyethyl)carbamateHCID 2733206—
EduktDiethyl azodicarboxylateHCID 5462977—
LösungsmittelTetrahydrofuranHCID 8028—
Produkttert-Butyl (2-azidoethyl)carbamateHCID 22323692107,4%

Reaktionsschritte

To a solution of (2-hydroxyethyl)carbamic acid t-butyl ester (1.5 g, 6.2 mmol) in tetrahydrofuran (75 ml) were added diphenylphosphoryl azide (3.0 ml, 13.9 mmol), triphenylphosphine (3.7 g, 14.1 mmol), and a 40% solution of diethylazodicarboxylate in toluene (5.1 g, 13.9 mmol) in an ice bath under an atmosphere of nitrogen, and then the mixture was stirred for 4 hours under the same conditions. After checking the completion of the reaction, the reaction mixture was partitioned between ethyl acetate and saturated aqueous sodium chloride solution. The organic layer was dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The obtained residue was purified by chromatography on a silica gel column using hexane:ethyl acetate (3:1) as the eluant to afford (2-azidoethyl)carbamic acid t-butyl ester (1.24 g, yield 72%) as a colorless and transparent syrup.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07001897B2
Quelldatensatzuspto-grants-2006_02
ORD IDord-eb5dae2d776a4ed383d3246376f54f68
Quellennotizuspto-grants-2006_02