Sodium Hydroxide → (2-Chloro-3-trifluoromethyl-benzyl)-cyclopropyl-amine

HRID 1096836Notes

Reaction equation

HRID 1096836 reaction equation
[Cl:1][C:2]1[C:9]([C:10]([F:13])([F:12])[F:11])=[CH:8][CH:7]=[CH:6][C:3]=1[CH:4]=O.[CH:14]1([NH2:17])[CH2:16][CH2:15]1.[BH4-].[Na+].[OH-].[Na+]>CO>[Cl:1][C:2]1[C:9]([C:10]([F:13])([F:12])[F:11])=[CH:8][CH:7]=[CH:6][C:3]=1[CH2:4][NH:17][CH:14]1[CH2:16][CH2:15]1

Participants

6

Procedure

The mixture of 2-chloro-3-trifluoromethylbenzaldehyde (37.4 g, 179.5 mmol) and cyclopropylamine (25.2 mL, 359.1 mmol) in MeOH (500 mL) was stirred at rt overnight. Subsequently, NaBH4 (9.2 g, 233.4 mmol) was added at 0° C. and the mixture was allowed to warm to rt overnight. 1M NaOH was added (100 mL) and the solvent was evaporated under reduced pressure. Brine (100 mL) was added and extracted with EtOAc (3×100 mL). 2N HCl (100 mL) was added and extracted with Et2O (3×100 mL). The org. phase was washed with 2N HCl (100 mL). To the combined water phase 2N NaOH was added (to pH=14) and the mixture was extracted with EtOAc (3×100 mL). The combined org. extracts were dried over MgSO4, filtered, and the solvents were removed under reduced pressure. The corresponding product was isolated as a colourless liquid (33.7 g, 75%). LC-MS: tR=0.66 min; ES+: 250.17.

Workup

  1. temperatureto warm to rt overnight
  2. customthe solvent was evaporated under reduced pressure
  3. additionBrine (100 mL) was added
  4. extractionextracted with EtOAc (3×100 mL)
  5. addition2N HCl (100 mL) was added
  6. extractionextracted with Et2O (3×100 mL)
  7. washphase was washed with 2N HCl (100 mL)
  8. additionTo the combined water phase 2N NaOH was added (to pH=14)
  9. extractionthe mixture was extracted with EtOAc (3×100 mL)
  10. dry with materialextracts were dried over MgSO4
  11. filtrationfiltered
  12. customthe solvents were removed under reduced pressure

Sources & evidence

ORD record
ord-d743df8f829d4cb7a58f8520e96ff591
Source dataset
uspto-grants-2012_03
Patent number
US08138340B2

Reaction notes

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