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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 383219Erstellt: 25. Oktober 2026

Methanol → 4-(1-Nitrobenzyl)pyridine

https://huagongshe.com/reaction/383219

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
EduktNADPHHCID 5884—
Edukt4-(4-Nitrobenzyl)pyridineHCID 14129—
EduktSodium HydroxideHCID 14798—
LösungsmittelPotassium Phosphate, TribasicHCID 62657—
LösungsmittelEthylacetate acetoneHCID 21584569—
Produkt4-(1-Nitrobenzyl)pyridineHCID 68671185—

Reaktionsschritte

A typical reaction contained enzyme (1.0 ml, 1×10−6 M) in potassium phosphate buffer (0.1 M, pH 8.0), alkene (1.0×10−3 M), and methanol (1%) in a vial. The reaction was initiated with NADPH (50 μl, 1.0×10−3 M), and allowed to stir aerobically for 5 minutes. 300 μl of a stock solution of 4-(4-nitrobenzyl)pyridine (5% w/w in acetone) was added to the reaction, and the vial was sealed. The reaction was incubated at 80° C. for 20 minutes and chilled on ice. 600 μl of an ethylacetate/acetone (5:2) solution and 300 μl 5 M aqueous NaOH was added to the reaction solution. The solution was mixed thoroughly, and the absorbance of the organic layer was measured at 540 nm in a glass 96-well plate with microplate spectrophotometer.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08367386B2
Quelldatensatzuspto-grants-2013_02
ORD IDord-6a2d41c281ab4b6aa97ff31a26cf2bba
Quellennotizuspto-grants-2013_02