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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 969481Erstellt: 24. Oktober 2026

Potassium Carbonate → Tert-butyl(4'-hydroxybiphenyl-3-ylmethyl)methylcarbamate

https://huagongshe.com/de/reaction/969481

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
Edukt4-Hydroxyphenylboronic acidHCID 2734360—
Edukttert-Butyl 3-bromobenzyl(methyl)carbamateHCID 20738487—
KatalysatorHCID 178420554HCID 178420554—
LösungsmittelWaterHCID 962—
Lösungsmittel1,2-DimethoxyethaneHCID 8071—
ProduktTert-butyl(4'-hydroxybiphenyl-3-ylmethyl)methylcarbamateHCID 6964326168%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

41.6 ml (83.2 mmol) of aqueous 2M potassium carbonate solution are added dropwise to a solution of 10 g (33 mmol) of tert-butyl (3-bromobenzyl)-N-methylcarbamate and 8.3 g (60 mmol) of 4-hydroxybenzeneboronic acid in 100 ml of ethylene glycol dimethyl ether. The reaction medium is degassed and 1.9 g (1.7 mmol) of tetrakis(triphenylphosphino)palladium are added. After heating for 12 hours at 80° C., the reaction medium is cooled, diluted with water and extracted with ethyl acetate. The organic phase is dried over sodium sulfate, filtered and concentrated under vacuum. The residue obtained is purified by chromatography on a column of silica eluted with an 80/20 heptane/ethyl acetate mixture. 7 g of tert-butyl (4′-hydroxybiphenyl-3-ylmethyl)methylcarbamate are obtained in the form of a beige-colored solid, in a yield of 68%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07307078B2
Quelldatensatzuspto-grants-2007_12
ORD IDord-1dfe92e2a34c44d4891e5ed515bff36e
Quellennotizuspto-grants-2007_12