HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitric Acid → 5-Chloro-4-methyl-2-nitrophenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | 3-Chloro-4-methylphenol | HCID 14853 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 5-Chloro-4-methyl-2-nitrophenol | HCID 13560303 | — |
Reaction Steps
245.0 g of 3A was mixed with 1.6 liters of glacial acetic acid, and the resulting solution was stirred at 8°-10° C. while 109.6 g of 90% aqueous nitric acid was added (two hours). The mixture was stirred at 10°-15° C. for five hours, poured over ice water and extracted with ether/hexane. The extract was washed with water, dried and stripped to dryness. The residue was stirred with 3 liters of hexane and the hexane solution was filtered through silica gel. The filtrate was held at -20° C. for 16 hours, filtered, and the filtrate was concentrated to one liter, charcoaled, then held at -30° to -35° C. for two hours and filtered. The solid products were combined to give 3-chloro-4-methyl-6-nitrophenol (3B).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04587259 |
| Source dataset | uspto-grants-1986_05 |
| ORD ID | ord-d8cb00fa749546bba0f24ce4bc3ebea3 |
| Source note | uspto-grants-1986_05 |