Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Aminophenol | HCID 5801 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 2-Acetamidophenol | HCID 11972 | — |
Reaction Steps
10.9 g of o-aminophenol and 100 ml of acetic acid were placed in a 300 ml round-bottom flask, followed by addition of 10.2 g acetic anhydride under ice-water cooling. The mixture was heated at 60° C. for one hour to complete the reaction, resulting in formation of 2-acetaminophenol. 23.4 g gaseous chlorine was then passed into the reaction mixture at a temperature of 80°-90° C. and the resulting reaction solution was cooled and evaporated under reduced pressure to leave 24.9 g of yellow crystals of 2-acetamino-4,5,6-trichlorophenol which melted with decomposition at 200° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04420486 |
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| Source dataset | uspto-grants-1983_12 |
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| ORD ID | ord-c6950884cad24000aa7b4df8e2166ff8 |
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| Source note | uspto-grants-1983_12 |
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