# US 5,344,979 A · Process for preparing color-stabilized acetaminophen > Agents: this data is available as JSON from the patentgrep API and MCP server — see https://patentgrep.com/llms.txt - Number: US 5,344,979 A - Document ID: US5344979A - Status: Granted - Kind: A - Application number: 08/054,733 - Filed: 1993-04-29 - Granted: 1994-09-06 - Earliest claimed: 1993-04-29 - Assignees: Hoechst Celanese Corporation - Inventors: Edward G. Zey; George A. Blay - Web page: https://patentgrep.com/patent/US5344979A ## CPC - C07C 231/24: Separation; Purification - C07C: ACYCLIC OR CARBOCYCLIC COMPOUNDS ## Abstract A method is provided for purifying a crude N-acetyl-para-aminophenol (APAP) containing color bodies or their precursors, the method comprising: a) forming a wet crude APAP; and b) subsequently drying said crude APAP in the presence of a sufficient amount of an acetylating agent for a sufficient period of time to convert said color bodies or their precursors to substantially non-color bodies. ## Claims ### Claim 1 A method of purifying a crude N-acetyl-para-aminophenol (APAP) containing color bodies or their precursors comprising forming a wet, crude APAP, and subsequently drying said crude APAP in the presence of a sufficient amount of an acetylating agent for a sufficient period of time to convert said color bodies or their precursors to substantially non-color bodies. ### Claim 2 (depends on 1) The method of claim 1 wherein said acetylating agent is acetic-propionic anhydride. ### Claim 3 (depends on 1) The method of claim 1 wherein said acetylating agent is acetyl chloride. ### Claim 4 (depends on 1) The method of claim 1 wherein said acetylating agent is phenyl acetate. ### Claim 5 (depends on 1) The method of claim 1 wherein said acetylating agent is ketene. ### Claim 6 (depends on 1) The method of claim 1 wherein said acetylating agent is acetic anhydride. ### Claim 7 (depends on 1) The method of claim 1 wherein said acetylating agent is present in an amount of from about 0.001% to about 2%, based on the weight of the crude APAP. ### Claim 8 (depends on 1) The process of claim 1 wherein the crude APAP is first treated with carbon and the carbon removed prior to contacting said crude APAP with said acetylating agent. ### Claim 9 In a method of preparing N-acetyl-para-aminophenol (APAP) which comprises the steps of reacting acetic anhydride with a mixture of p-aminophenol and water, cooling the reaction mixture to precipitate the APAP, filtering to remove excess acetic acid, neutralizing the wet APAP with ammonium hydroxide, and agitating the resulting solution with carbon black, the improvement which comprises adding sufficient quantities of an acetylating agent to the crude APAP at any point after the formation of said crude APAP whereby the color bodies or their precursors in said crude APAP will be substantially converted to non-color bodies. ### Claim 10 In a process of preparing an N-acyl-hydroxy aromatic amine which comprises the steps of contacting a hydroxy aromatic ketone with a hydroxylamine salt and a base to form the ketoxime of said ketone, and contacting said ketoxime with a Beckmann rearrangement catalyst to form said crude aromatic amine containing color bodies or their precursors, the improvement which comprises contacting said crude aromatic amine with an acetylating agent for a sufficient period of time to convert said color bodies or their precursors to substantially non-color bodies. ### Claim 11 In a method of preparing N-acetyl-para-aminophenol (APAP) which comprises the steps of reacting 4-hydroxyacetophenone with a hydroxylamine salt and a base to obtain 4-hydroxyacetophenone oxime and then subjecting the 4-hydroxyacetophenone oxime to a Beckmann rearrangement in the presence of a catalyst to form the crude APAP containing color bodies or their precursors, the improvement which comprises contacting said crude APAP with an acetylating agent for a sufficient period of time to convert said color bodies or their precursors to substantially non-color bodies. ### Claim 12 (depends on 11) The method of claim 11 wherein said acetylating agent is acetic-propionic anhydride. ### Claim 13 (depends on 11) The method of claim 11 wherein said acetylating agent is acetyl chloride. ### Claim 14 (depends on 11) The method of claim 11 wherein said acetylating agent is phenyl acetate. ### Claim 15 (depends on 11) The method of claim 11 wherein said acetylating agent is ketene. ### Claim 16 (depends on 11) The method of claim 11 wherein said acetylating agent is acetic anhydride. ### Claim 17 (depends on 11) The method of claim 11 wherein said acetylating agent is present in an amount of from about 0.001% to about 2%, based on the weight of the crude APAP. ### Claim 18 (depends on 11) The method of claim 11 wherein the crude APAP is first treated with carbon and the carbon removed prior to contacting said crude APAP with said acetylating agent. ### Claim 19 (depends on 11) The method of claim 11 wherein the contacting step is carried out in a fluidized bed wherein said crude APAP is dried at a temperature of at least 40.degree. C. ### Claim 20 (depends on 19) The method of claim 19 wherein the fluidized bed is maintained by an inert gas. ### Claim 21 (depends on 11) The method of claim 11 wherein said acetylating agent is present in an amount of from about 0.01% to about 5.0% based on the weight of the crude APAP.