Benzhydrylamine → HCID 10729452, compound

HRID 537377Notes

Reaction equation

HRID 537377 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]=1

Participants

5

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

  1. additionA 100-mL round-bottomed flask containing a stir bar
  2. customThe flask was capped with a plastic stopper
  3. stirringthe mixture was stirred at room temperature
  4. customafter 5 min
  5. stirringAfter stirring for 1 h
  6. customthe mixture was decanted into a 200 mL round-bottomed flask
  7. washrinsing with CH2Cl2 (4×5 mL)
  8. concentrationconcentrated to 8-10 mL
  9. customa rotary evaporator
  10. temperatureThe flask was then maintained at 1 torr for 10 min
  11. customtransferred to a 250-mL separatory funnel
  12. washwashed with NaHCO3 (50 mL)
  13. dry with materialThe organic layer was dried over Na2SO4
  14. filtrationfiltered through a medium porosity
  15. customfitted disk funnel into a 200-mL round-bottomed flask
  16. concentrationconcentrated in vacuo (30 torr→1 torr)
  17. customto provide a pale yellow oil that solidified to a white solid within 5 min at 1 torr
  18. 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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