HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 4-[2-Methyl-5-(methyloxy)-4-nitrophenyl]-1-propyl-1,2,3,6-tetrahydropyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 4-[2-Methyl-5-(methyloxy)-4-nitrophenyl]-1-propylpyridinium iodide | HCID 66649759 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-[2-Methyl-5-(methyloxy)-4-nitrophenyl]-1-propyl-1,2,3,6-tetrahydropyridine | HCID 59452927 | 96% |
Reaction Steps
To 4-[2-methyl-5-(methyloxy)-4-nitrophenyl]-1-propylpyridinium iodide (1.04 g, 2.51 mmol) in 25 mL of MeOH at 0° C. was added, NaBH4 (0.284 g, 7.53 mmol) over 1 h. The mixture was allowed to come to rt over 2 h. The solvent was reduced to approximately 5 mL and then diluted with EtOAc, washed with conc. NaHCO3, dried (Na2SO4), filtered, rotovaped down, and purified by flash chromatography to give the title compound of step C (0.7 g, 2.41 mmol, 96%). 1H NMR (400 MHz, DMSO-d6) δ ppm 7.71 (s, 1H), 7.00 (s, 1H), 5.61-5.67 (m, 1H), 3.87 (s, 3H), 2.98-3.07 (m, 2H), 2.60 (t, J=5.50 Hz, 2H), 2.28-2.37 (m, 4H), 2.20 (s, 3H), 1.43-1.53 (m, 2H), 0.87 (t, J=7.52 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08093239B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-e1b6302e8efe401ea84425c03e39d657 |
| Source note | uspto-grants-2012_01 |