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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 38116Erstellt: 23. Oktober 2026

Water → Tert-butyl(trans)-2-(1,1'-biphenyl-4-yl)cyclopropylcarbamate

https://huagongshe.com/de/reaction/38116

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktPotassium CarbonateHCID 11430—
EduktBoronic AcidHCID 61668—
Edukttert-butyl ((1R,2S)-2-(4-bromophenyl)cyclopropyl)carbamateHCID 86658779—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelAcetonitrile--water (1/1)HCID 18373917—
ProduktTert-butyl(trans)-2-(1,1'-biphenyl-4-yl)cyclopropylcarbamateHCID 86658778—

Reaktionsschritte

A solution of tert-butyl(trans)-2-(4-bromophenyl)cyclopropylcarbamate (Intermediate F; 1 equiv), 1.2 equiv of the boronic acid, 3.0 equiv of K2CO3 in CH3CN+H2O (4:1) was degassed for 30 mins with Argon gas, added 0.01 equiv of Pd (PPh3)4, heated the reaction mixture at reflux temp for 4 h. The progress of the reaction was monitored by TLC, after completion, poured the reaction mixture into water, extracted with EtOAc. The combined extracts were washed with water, brine, dried over anhydrous Na2SO4, filtered and evaporated. The crude residue was purified by column chromatography to get tert-butyl(trans)-2-(1,1′-biphenyl-4-yl)cyclopropylcarbamate derivative

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08524717B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-40bdd2650dc84da68d73597eb7e292c0
Quellennotizuspto-grants-2013_09