HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitric Acid → 1,3-Bis(2-chloro-alpha,alpha,alpha-trifluoro-p-tolyloxy)-4-nitrobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | 1,3-Bis(2-chloro-alpha,alpha,alpha-trifluoro-p-tolyloxy)benzene | HCID 86735305 | — |
| Solvent | Benzene--water (1/1) | HCID 22272175 | — |
| Product | 1,3-Bis(2-chloro-alpha,alpha,alpha-trifluoro-p-tolyloxy)-4-nitrobenzene | HCID 86735304 | — |
Reaction Steps
1,3-Bis(2-chloro-α,α,α-trifluoro-p-tolyloxy)benzene (12 g. 0.0255 mole) is added to a mixture of concentrated nitric acid (12 g.) and sulfuric acid (15 g.) at 5° C. The temperature is then allowed to rise to 25°-30° C. with manual stirring and mild ice bath cooling and after 10-20 minutes, the oil solidifies. The mixture is taken up in water/benzene (400 ml)/hexane (400 ml) and the organic phase is washed with water, dried, filtered through activated silica gel (~20 g.), and the solvents removed. The residue is recrystallized from isopropanol to give 1,3-bis(2-chloro-α,α,α-trifluoro-p-tolyloxy)-4-nitrobenzene, (7.4 g. 56%) m.p. 110°-111.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04220468 |
| Source dataset | uspto-grants-1980_09 |
| ORD ID | ord-4ae9ad4c84a74ddb99cfef1f5ccc5ab8 |
| Source note | uspto-grants-1980_09 |