Reaction equation
S(=O)(=O)(O)O.[Cl:6][C:7]1[CH:8]=[CH:9][C:10]([OH:17])=[C:11]([NH:13][C:14](=[O:16])[CH3:15])[CH:12]=1.[N+:18]([O-])([OH:20])=[O:19]>O>[Cl:6][C:7]1[CH:8]=[C:9]([N+:18]([O-:20])=[O:19])[C:10]([OH:17])=[C:11]([NH:13][C:14](=[O:16])[CH3:15])[CH:12]=1Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 25 °C
Procedure
224.5 g of sulphuric acid (50% w/w) was dissolved in 300 ml of water and cooled to 25° C. while stirring under a mild nitrogen purge. 185.1 g (1 mole) of N-(5-chloro-2-hydroxyphenyl)acetamide prepared according to Example 1a was added to the diluted sulphuric acid and mixed intensively. 4 ml of nitric acid 65% w/w was added to the foam formed on top of the reaction mixture at low stirring speed. The stirring speed was increased and 75 ml of nitric acid 65% w/w was added in 45 minutes, while maintaining the temperature between 23 and 26° C. The mixture was stirred vigorously for an additional 1 hour at 23-26° C. Then the mixture was cooled to 0-5° C. and vigorously stirred at this temperature for 1 hour. The solid was filtered off quickly, washed three times with 300 ml of cold water, sucked for at least 30 minutes and dried at 50° C. and 100 mbar under a gentle nitrogen stream till dry.
Workup
- custompurge
- additionmixed intensively
- customformed on top of the reaction mixture at low stirring speed
- temperatureThe stirring speed was increased
- temperaturewhile maintaining the temperature between 23 and 26° C
- stirringThe mixture was stirred vigorously for an additional 1 hour at 23-26° C
- temperatureThen the mixture was cooled to 0-5° C.
- stirringvigorously stirred at this temperature for 1 hour
- filtrationThe solid was filtered off quickly
- washwashed three times with 300 ml of cold water
- waitsucked for at least 30 minutes
- customdried at 50° C.
- customtill dry
Sources & evidence
- ORD record
- ord-ccd13ade850745d4aaf7dc82903a0142
- Source dataset
- uspto-grants-2008_09
- Patent number
- US07423040B2
Linked notes
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