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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383219Generated: October 25, 2026

Methanol → 4-(1-Nitrobenzyl)pyridine

https://huagongshe.com/reaction/383219

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantNADPHHCID 5884—
Reactant4-(4-Nitrobenzyl)pyridineHCID 14129—
ReactantSodium HydroxideHCID 14798—
SolventPotassium Phosphate, TribasicHCID 62657—
SolventEthylacetate acetoneHCID 21584569—
Product4-(1-Nitrobenzyl)pyridineHCID 68671185—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367386B2
Source datasetuspto-grants-2013_02
ORD IDord-6a2d41c281ab4b6aa97ff31a26cf2bba
Source noteuspto-grants-2013_02