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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 74001Erstellt: 24. Oktober 2026

Methyl chlorodifluoroacetate → 1-Tert-butyl-2-(benzyloxy)-5-(trifluoromethyl)-4-nitrobenzene

https://huagongshe.com/de/reaction/74001

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl chlorodifluoroacetateHCID 73935—
EduktPotassium BromideHCID 253877—
EduktPotassium FluorideHCID 522689—
Edukt1-Tert-butyl-2-(benzyloxy)-5-bromo-4-nitrobenzeneHCID 57470237—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
Produkt1-Tert-butyl-2-(benzyloxy)-5-(trifluoromethyl)-4-nitrobenzeneHCID 5747023867%

Reaktionsbedingungen

Temperatur125 °C

Reaktionsschritte

A mixture of 1-tert-butyl-2-(benzyloxy)-5-bromo-4-nitrobenzene (913 mg, 2.5 mmol), KF (291 mg, 5 mmol), KBr (595 mg, 5 mmol), CuI (570 mg, 3 mmol), methyl chlorodifluoroacetate (1.6 mL, 15 mmol) and DMF (5 mL) was stirred at 125° C. in a sealed tube overnight, cooled to room temperature, diluted with water and extracted three times with EtOAc. The combined organic layers were washed with brine and dried over anhydrous MgSO4. After removal of the solvent, the residue was purified by column chromatography (0-5% EtOAc-Hexane) to yield 1-tert-butyl-2-(benzyloxy)-5-(trifluoromethyl)-4-nitrobenzene (591 mg, 67%). 1H NMR (400 MHz, CDCl3) 7.66 (s, 1H), 7.37 (m, 5H), 7.19 (s, 1H), 5.21 (s, 2H), 1.32 (s, 9H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08829204B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-0e2a8034158147ecb0e8840e9ae30b7d
Quellennotizuspto-grants-2014_09