Benzhydrylamine → HCID 10729452, compound
Reaction equation
[O-]S([O-])(=O)=O.[Na+].[Na+].[CH3:8][C:9]([CH3:13])([CH3:12])[CH:10]=O.[NH2:14][CH:15]([C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1)[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1>C(Cl)Cl>[CH3:8][C:9]([CH3:13])([CH3:12])[CH:10]=[N:14][CH:15]([C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)[C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A 100-mL round-bottomed flask containing a stir bar was charged with Na2SO4 (8.0 g) and CH2Cl2 (40 mL). Trimethylacetaldehyde (8) (7.65 mL, 52 mmol, 1.3 equiv) and aminodiphenylmethane (9) (6.89 mL, 40 mmol, 1.0 equiv) were added sequentially via syringe while stirring. The flask was capped with a plastic stopper, and the mixture was stirred at room temperature. The mixture became cloudy after 5 min. After stirring for 1 h, the mixture was decanted into a 200 mL round-bottomed flask, rinsing with CH2Cl2 (4×5 mL), and concentrated to 8-10 mL using a rotary evaporator. The flask was then maintained at 1 torr for 10 min. The resulting pale yellow solid was taken up in CH2Cl2 (50 mL), transferred to a 250-mL separatory funnel, and washed with NaHCO3 (50 mL). The organic layer was dried over Na2SO4, filtered through a medium porosity fitted disk funnel into a 200-mL round-bottomed flask, and concentrated in vacuo (30 torr→1 torr) to provide a pale yellow oil that solidified to a white solid within 5 min at 1 torr. The solid was broken up into approximately 1-cm diameter pieces using a spatula, and was maintained at 1 torr for another 15 min to provide N-(2,2 dimethylpropylidene) diphenylmethanamine (2a) as a white solid in approximately 98% 1H-NMR purity. The product was used in the next step without further purification. Yield: 9.79 g (38.9 mmol, 97%).
Workup
- additionA 100-mL round-bottomed flask containing a stir bar
- customThe flask was capped with a plastic stopper
- stirringthe mixture was stirred at room temperature
- customafter 5 min
- stirringAfter stirring for 1 h
- customthe mixture was decanted into a 200 mL round-bottomed flask
- washrinsing with CH2Cl2 (4×5 mL)
- concentrationconcentrated to 8-10 mL
- customa rotary evaporator
- temperatureThe flask was then maintained at 1 torr for 10 min
- customtransferred to a 250-mL separatory funnel
- washwashed with NaHCO3 (50 mL)
- dry with materialThe organic layer was dried over Na2SO4
- filtrationfiltered through a medium porosity
- customfitted disk funnel into a 200-mL round-bottomed flask
- concentrationconcentrated in vacuo (30 torr→1 torr)
- customto provide a pale yellow oil that solidified to a white solid within 5 min at 1 torr
- temperaturewas maintained at 1 torr for another 15 min
Sources & evidence
- ORD record
- ord-77119fabbdc846e9ad54606e5b1de6c5
- Source dataset
- uspto-grants-2014_10
- Patent number
- US08859812B2
Reaction notes
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