Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 254815Erstellt: 26. Oktober 2026

Dimethylformamide → N,N,N',N'-Tetramethylazodicarboxamide

https://huagongshe.com/reaction/254815

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktTriethylamineHCID 8471—
EduktOxalyl chlorideHCID 65578—
Edukt2,2-DimethylpropanehydrazideHCID 545147—
LösungsmittelDichloromethaneHCID 6344—
ProduktN,N,N',N'-TetramethylazodicarboxamideHCID 427861%

Reaktionsschritte

To the solution of acid (63) (330 mg, 0.74 mmol) in CH2Cl2 (10 mL) was added oxalyl chloride (77 μL, 0.88 mmol) and the catalytic amount of DMF. The reaction mixture was stirred for 1 hr and concentrated in vacuo. The residue (crude acyl chloride) was diluted with CH2Cl2 (10 mL) and pivalohydrazide (128 mg, 1.10 mmol) and triethylamine (0.31 mL, 2.21 mmol) was added. The reaction mixture was stirred for 2 hrs at room temperature. The reaction mixture was concentrated in vacuo and diluted with EtOAc (50 mL). The organic layer was washed with aq. 1N HCl and aq. sat'd NaHCO3 solution, dried over anhydrous MgSO4, filtered, and concentrated in vacuo. Purification by Prep-LC (Gilson) provided 244 mg (61%) of desired diamide as solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07875647B2
Quelldatensatzuspto-grants-2011_01
ORD IDord-55edbabeaad54a1ab3564d665f61bf4d
Quellennotizuspto-grants-2011_01