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HRID 23610Erstellt: 24. Oktober 2026

Triethylamine → di-tert-butyl (2,3,4,5-tetrafluorobenzoyl)-L-glutamate

https://huagongshe.com/de/reaction/23610

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktDi-tert-butyl glutamate hydrochlorideHCID 208636—
Edukt2,3,4,5-Tetrafluorobenzoyl chlorideHCID 2733689—
LösungsmittelDichloromethaneHCID 6344—
Produktdi-tert-butyl (2,3,4,5-tetrafluorobenzoyl)-L-glutamateHCID 11270493—

Reaktionsschritte

To an ice-cold solution of di-tert-butyl L-glutamate hydrochloride (6.6 g, 22.4 mmol) and Et3N (6.9 ml, 50 mmol) in dry CH2Cl2 (70 ml) was added, over a period of 1.5 hr, 2,3,4,5-tetrafluorobenzoyl chloride (5.0 g, 23.5 mmol) in dry CH2Cl2 (20 ml) and thirty minutes later the solution was allowed to warm to room temperature. Sixteen hours later the solution was washed with H2O, dried (MgSO4) and evaporated to dryness. 1H NMR δ 1.40+1.42 (2s, 18H, t-butyl), 1.85+1.95 (2m, 2H, CH2CH), 2.34 (t, 2H, CH2CO, J=7.5 Hz), 4.3 (m, 1H, CH), 7.57 (m, 1H, H6), 8.80 (d, 1H, NH, J=7.5 Hz); 19F NMR δ −138.6+139.0 (2m, 2F, F2+5), −152.4 (m, 1H, F4), −154.9 (t, 1F, F3, J=20 Hz).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06852755B1
Quelldatensatzuspto-grants-2005_02
ORD IDord-b2e52de445c646f1a9a2145db1d992a4
Quellennotizuspto-grants-2005_02