Hydrochloric Acid → HCID 178423975, compound
Reaction equation
[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([C:10]([C:12]2[CH:17]=[CH:16][C:15]([CH3:18])=[CH:14][CH:13]=2)=O)=O)=[CH:4][CH:3]=1.Cl.[NH2:20][CH2:21][C:22]([NH2:24])=[O:23].[OH-].[Na+].Cl.C(=O)(O)[O-].[K+]>O.CO>[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[N:20]=[CH:21][C:22]([OH:23])=[N:24][C:10]=2[C:12]2[CH:17]=[CH:16][C:15]([CH3:18])=[CH:14][CH:13]=2)=[CH:4][CH:3]=1Participants
8
Reactant 5
Product 1
Reagents, catalysts & solvents 2
Procedure
First, 5.5 g (23 mmol) of 4,4′-dimethylbenzil, 3.1 g (28 mmol) of glycinamide hydrochloride, 2.2 g (55 mmol) of sodium hydroxide, and 120 mL of methanol were put into a three-neck flask equipped with a reflux pipe, the air in the flask was replaced with nitrogen, and the mixture was refluxed for 8.5 hours. Then, stirring was performed until the temperature of the flask was returned to room temperature. After that, 3 mL of 12 M concentrated hydrochloric acid, 2.3 g of potassium bicarbonate, and 58 mL of water were added to this mixture, and filtration was performed.
Workup
- customequipped with a reflux pipe
- temperaturethe mixture was refluxed for 8.5 hours
- customwas returned to room temperature
Sources & evidence
- ORD record
- ord-bbc4e62e13ef41d0acf8a22fbb26a998
- Source dataset
- uspto-grants-2016_01
- Patent number
- US09231217B2
Reaction notes
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