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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1449577Erstellt: 25. Oktober 2026

Carbon Dioxide → 2-(tert-Butoxycarbonyl)-6-chloro-4-trifluoromethylbenzoic acid

https://huagongshe.com/reaction/1449577

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCarbon DioxideHCID 280—
EduktWaterHCID 962—
EduktTetrahydrofuranHCID 8028—
Edukttert-butyl N-[3-chloro-5-(trifluoromethyl)phenyl]carbamateHCID 18929880—
EduktHCID 178418306HCID 178418306—
LösungsmittelPentaneHCID 8003—
Produkt2-(tert-Butoxycarbonyl)-6-chloro-4-trifluoromethylbenzoic acidHCID 1892994782%

Reaktionsbedingungen

Temperatur-75 °C

Reaktionsschritte

To a cold (-100° C.) stirred solution of N-(tert-butoxycarbonyl)-3-chloro-5-trifluoromethylaniline 93.4 g, 11.5 mM) in dry tetrahydrofuran (30 mL) under a nitrogen atmosphere was added dropwise t-butyllithium (14.2 mL of 1.7M solution, 24.2 mM) in pentane. The temperature of the reaction mixture was maintained at -103° to -98° C. during the addition and for 3.25 hr after the addition was completed. Crushed Dry Ice was then added to the cold reaction mixture which, after being allowed to warm to -75° C., was poured into water. The resulting mixture was extracted with ethyl acetate and the combined extracts were dried (MgSO4), filtered and concentrated to leave (3.2 g, 82%) the title compound as a solid white foam.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05599814
Quelldatensatzuspto-grants-1997_02
ORD IDord-fbe886a1c4e449dc8d59f3693e9f7c69
Quellennotizuspto-grants-1997_02