Dimethylformamide dimethyl acetal → HCID 66823376, compound
Reaction equation
[C:1]([O:5][C:6](=[O:29])[NH:7][C:8]1([C:14]2[CH:19]=[CH:18][C:17]([C:20](=[O:28])[CH2:21][C:22]3[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=3)=[CH:16][CH:15]=2)[CH2:11][C:10]([OH:13])([CH3:12])[CH2:9]1)([CH3:4])([CH3:3])[CH3:2].[CH3:30][N:31]([CH:33](OC)OC)[CH3:32]>C1(C)C=CC=CC=1>[C:1]([O:5][C:6](=[O:29])[NH:7][C:8]1([C:14]2[CH:15]=[CH:16][C:17]([C:20](=[O:28])[C:21]([C:22]3[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=3)=[CH:30][N:31]([CH3:33])[CH3:32])=[CH:18][CH:19]=2)[CH2:9][C:10]([OH:13])([CH3:12])[CH2:11]1)([CH3:2])([CH3:3])[CH3:4]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of compound 2-3 (3.96 g, 10 mmol) in toluene (20 mL) was added DMFDMA (9.2 g, 35 mmol) and the mixture was heated at reflux for 4 hours. The mixture was cooled and the formed white solid was collected. After washed by PE, the solid was dried in vacuum to get the product 2.
Workup
- temperaturethe mixture was heated
- temperatureat reflux for 4 hours
- temperatureThe mixture was cooled
- customthe formed white solid was collected
- washAfter washed by PE
- customthe solid was dried in vacuum
Sources & evidence
- ORD record
- ord-707847a1e62f4ff79a5973454c5b71b9
- Source dataset
- uspto-grants-2014_04
- Patent number
- US08691825B2
Reaction notes
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