HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 4-(1-Nitrobenzyl)pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | NADPH | HCID 5884 | — |
| Reactant | 4-(4-Nitrobenzyl)pyridine | HCID 14129 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Solvent | Ethylacetate acetone | HCID 21584569 | — |
| Product | 4-(1-Nitrobenzyl)pyridine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08367386B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-6a2d41c281ab4b6aa97ff31a26cf2bba |
| Source note | uspto-grants-2013_02 |