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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1296217Erstellt: 26. Oktober 2026

Sodium Formate → Tert-butyl (5-formyl-2-methoxybenzyl)carbamate

https://huagongshe.com/reaction/1296217

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium FormateHCID 2723810—
EduktTert-butyl (5-bromo-2-methoxybenzyl)carbamateHCID 22926030—
KatalysatorTriphenylphosphineHCID 11776—
KatalysatorHCID 178418476HCID 178418476—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelEthyl AcetateHCID 8857—
LösungsmittelHCID 178418416HCID 178418416—
ProduktTert-butyl (5-formyl-2-methoxybenzyl)carbamateHCID 2249393175,1%

Reaktionsschritte

1.015 g of t-butyl N-(5-bromo-2-methoxybenzyl)carbamate, 45 mg of dichlorobis(triphenylphosphine)palladium (II), 330 mg of sodium formate and 17 mg of triphenylphosphine were dissolved in anhydrous N,N-dimethylformamide, followed by stirring for 2 hours at 110° C. in carbon monoxide atmosphere. The reaction mixture was diluted with ethyl acetate, and washed with water and saturated sodium bicarbonate water. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was evaporated. The residue was purified by silica gel column chromatography, and 640 mg of t-butyl N-(5-formyl-2-methoxybenzyl)carbamate was obtained from fractions eluted with hexane-ethyl acetate (3:1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07244861B2
Quelldatensatzuspto-grants-2007_07
ORD IDord-04a0c5bca7cd4ea2a1e72ff93846ae5a
Quellennotizuspto-grants-2007_07