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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 56121Erstellt: 23. Oktober 2026

Sodium Iodide → Tert-butyl (3-morpholinophenyl)carbamate

https://huagongshe.com/de/reaction/56121

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium IodideHCID 5238—
EduktBis(2-chloroethyl) etherHCID 8115—
EduktPotassium CarbonateHCID 11430—
Edukttert-butyl N-(3-aminophenyl)carbamateHCID 12877220—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
ProduktTert-butyl (3-morpholinophenyl)carbamateHCID 10104312558,3%

Reaktionsbedingungen

Temperatur150 °C

Reaktionsschritte

To a suspension of tert-butyl (3-aminophenyl)carbamate (7.59 g, 36.40 mmol), K2CO3 (10.06 g, 72.80 mmol) and NaI (16.37 g, 109.20 mmol) in DMF (300 mL) was added 2,2′-dichlorodiethyl ether (5.73 g, 40.1 mmol) slowly at 150° C. under N2. The reaction mixture was stirred at 150° C. overnight, then cooled to rt, poured into water (700 mL) and extracted with CH2Cl2 (200 mL×3). The combined organic phases were washed with water (200 mL×3) and brine (200 mL), dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by a silica gel column chromatography (PE/EtOAc (V/V)=4:1) to give the title compound as a yellow solid (5.91 g, 58%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09434695B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-02c84d3d9b0546dbbe946147c6594b9c
Quellennotizuspto-grants-2016_09