HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodine → 4-(Benzyloxy)-3-methoxy-2-nitrobenzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | 4-(Benzyloxy)-3-methoxy-2-nitrobenzaldehyde | HCID 561817 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(Benzyloxy)-3-methoxy-2-nitrobenzonitrile | HCID 58219845 | 95% |
Reaction Steps
Iodine (272 g, 1.1 mmol) was added to a mixture of 4-(benzyloxy)-3-methoxy-2-nitrobenzaldehyde (220 g, 766 mmol) and ammonium hydroxide (28% solution, 3 L) dissolved in THF (5 L). After 16 h the reaction mixture was treated with sodium sulfite (49 g, 383 mmol) and concentrated under reduced pressure to afford a thick slurry. The slurry was filtered, washed with water (250 mL) and dried to afford 4-(benzyloxy)-3-methoxy-2-nitrobenzonitrile as a solid (206 g, 95%): 1H NMR (DMSO-d6) δ: 7.89 (1H, d), 7.59 (1H, d), 7.49 (2H, m), 7.40 (3H, m), 5.35 (2H, s), 3.91 (3H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08895549B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-bf63010067dd4dfab4224d22e0ed6af9 |
| Source note | uspto-grants-2014_11 |