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HRID 77348Erstellt: 25. Oktober 2026

N,N-Bis(trimethylsilyl)trifluoroacetamide → HCID 178454638, Verbindung

https://huagongshe.com/reaction/77348

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN,N-Bis(trimethylsilyl)trifluoroacetamideHCID 65279—
EduktTrimethylsilyl iodideHCID 85247—
Eduktpentachlorophenyl (2E)-3-[4-[(diethoxyphosphinyl)oxy]phenyl]-but-2-enoateHCID 53248609—
LösungsmittelDichloromethaneHCID 6344—
ProduktHCID 178454638HCID 178454638—

Reaktionsschritte

Iodotrimethylsilane (2.0 mL, 14.2 mmol) in 5 mL of dry CH2Cl2 was added dropwise to a solution of 11b1 (2.0 g, 3.55 mmol) and bis(trimethylsilyl)trifluoroacetamide (1.8 mL, 7.1 mmol) in 20 mL of dry CH2Cl2 at 0° C. under argon. Stirring was continued for 1 h at 0° C. and 1 h at room temperature. The solution was concentrated in vacuo. The residue was treated with 20 mL of MeCN/H2O (9:1) and 5 drops of conc. HCl for 30 min and concentrated in vacuo. Toluene (5 mL) was added and evaporated twice. On addition of Et2O solids separated, which were collected by filtration and washed with the same solvent to give, after drying over P2O5 in vacuo, 1.6 g of 12b as a white powder (88%). It was used without further purification. 1H NMR (DMSO-d6, 300 MHz) δ 2.6 (s, 3H), 6.6 (s, 1H), 7.24 (d, J=8.7 Hz, 2H), 7.75 (d, J=8.7 Hz, 2H). HRMS (M+H) calc, 503.8658; found, 503.8691.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08841257B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-7aea457f0902405aa533806e6b5f45be
Quellennotizuspto-grants-2014_09