Hydrochloric Acid → HCID 10178135, compound
Reaction equation
[CH:1]1[CH:6]=[C:5]([S:7]([OH:10])(=[O:9])=[O:8])[CH:4]=[C:3]([NH2:11])[CH:2]=1.[CH2:12]([O:14][C:15](=[O:29])[CH:16]([C:21](=O)[C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1)[CH2:17][C:18](=O)[CH3:19])[CH3:13].[OH-].[Na+].CC1C=CC(S(O)(=O)=O)=CC=1.Cl>C(O)C>[CH2:12]([O:14][C:15]([C:16]1[CH:17]=[C:18]([CH3:19])[N:11]([C:3]2[CH:2]=[CH:1][CH:6]=[C:5]([S:7]([OH:10])(=[O:8])=[O:9])[CH:4]=2)[C:21]=1[C:22]1[CH:23]=[CH:24][CH:25]=[CH:26][CH:27]=1)=[O:29])[CH3:13]Participants
7
Procedure
Metanilic acid (5 mmol, 0.2 g), 2-benzoyl-4-oxo-pentanoic acid ethyl ester (5 mmol, 1.2 g), sodium hydroxide (5 mmol, 0.2 g), and tosic acid (0.1 g) were combined in ethanol, then heated under reflux. The resulting oil was treated with HCl (hydrochloric acid) at 0° C. to 5° C. to precipitate the unreacted metanilic acid. The remaining material was concentrated under vacuum and purified over silica gel. The named product was collected as brown crystals (m.p. 91° C.-92.5° C.)
Workup
- temperatureheated
- temperatureunder reflux
- customto precipitate the unreacted metanilic acid
- concentrationThe remaining material was concentrated under vacuum
- custompurified over silica gel
- customThe named product was collected as brown crystals (m.p. 91° C.-92.5° C.)
Sources & evidence
- ORD record
- ord-4b5fb80a27184b42bb074163ab16ea88
- Source dataset
- uspto-grants-2002_04
- Patent number
- US06372777B1
Reaction notes
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