HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856640Generated: October 30, 2026
Dimethyl Sulfoxide → HCID 22938350, compound
https://huagongshe.com/reaction/856640
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | 2-(4-Fluorobenzoyl)-3-propoxypyridine | HCID 22938851 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 22938350 | HCID 22938350 | 63.5% |
Reaction Steps
A solution of 2-(4-fluorobenzoyl)-3-propoxypyridine (4.46 g) and sodium azide (3.34 g) in. DMSO (50 ml) was stirred for 22 hours at 90° C. To the reaction mixture was added water, and the mixture was extracted with diethylether. The organic layer was washed with saturated brine, dried over magnesium sulfate and concentrated under reduced pressure, and a solution of the residue (4.8 g) in THF (50 ml) was added dropwise to a suspension of aluminum lithium hydride (1.3 g) in. THF (40 ml) at 0° C. The mixture was stirred at room temperature for 30 minutes, water (1.3 ml), 15% aqueous solution of sodium hydroxide (1.3 ml) and water (3.9 ml) were sequentially and slowly added dropwise to the solution at 0° C. The mixture was stirred at room temperature for 2 hours, magnesium sulfate was added to the mixture, and the precipitates were removed by filtration (Celite). The reaction mixture was concentrated under reduced pressure, and the residue was recrystallized from ethyl acetate to give (4-aminophenyl)(3-propoxypyridin-2-yl)methanol (2.82 g) as pale yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07262185B2 |
|---|
| Source dataset | uspto-grants-2007_08 |
|---|
| ORD ID | ord-e9c7cf1dce374e60a0ccdcb90cccebb1 |
|---|
| Source note | uspto-grants-2007_08 |
|---|