HuagongsheHuagongshe Chemistry Print Report · For research reference only
O-Xylene → 2-Hydroxy-2'nitro3,4'-diphenyl-5-tert-octylazobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | O-Xylene | HCID 7237 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Phenyl-4-tert-octylphenol | HCID 345941 | — |
| Reactant | 4-Phenyl-2-nitrobenzenediazonium hydrogen sulfate | HCID 85822691 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-Hydroxy-2'nitro3,4'-diphenyl-5-tert-octylazobenzene | HCID 136377676 | 25.8% |
Reaction Steps
To a solution of sodium hydroxide (12 g, 0.3 mol) and 2-phenyl-4-tert-octylphenol (14.1 g, 0.05 mol) in 150 mL of methanol maintained at 0–5° C. is added portionwise over 1.25 hours 4-phenyl-2-nitrobenzenediazonium hydrogen sulfate (30.6 g, 0.065 mol), prepared in (C) above. The reaction mixture is stirred for two hours at 0–5° C. Xylene (200 mL) is added to the reaction mixture. The organic phase is separated and extracted with water (4×200 mL). The organic phase is filtered and the solvent removed by distillation under an atmosphere of nitrogen. The residue is purified by flash chromatography (90:10 heptane:ethyl acetate eluent) to give 6.56 g of the title compound as a viscous dark red liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07148274B2 |
| Source dataset | uspto-grants-2006_12 |
| ORD ID | ord-ab70b0b742964b59aba510f9baa657ad |
| Source note | uspto-grants-2006_12 |