Hydrochloric Acid → 3-(Aminomethyl)-2-chlorobenzonitrile

HRID 1481341Notes

Reaction equation

HRID 1481341 reaction equation
Br[CH2:2][C:3]1[C:4]([Cl:11])=[C:5]([CH:8]=[CH:9][CH:10]=1)[C:6]#[N:7].[N-:12]=[N+]=[N-].[Na+].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.Cl>CN(C=O)C.CCOC(C)=O>[Cl:11][C:4]1[C:5]([C:6]#[N:7])=[CH:8][CH:9]=[CH:10][C:3]=1[CH2:2][NH2:12]

Participants

7

Procedure

To a solution of 3-(bromomethyl)-2-chlorobenzonitrile (0.87 mmol) in 9 mL DMF was added NaN3 (1.3 mmol) and the resulting brown solution was stirred at RT for 20 min. The reaction mixture was diluted with EtOAc, washed twice with water and brine, dried over MgSO4 and concentrated in vacuo. The crude azide was redissolved in 4.3 mL THF and 0.1 mL water. Triphenylphosphine (1.04 mmol) was added and the mixture was stirred at RT overnight. The reaction mixture was acidified with 0.1N HCl solution until pH 3 and it was extracted 3 times with Et2O. The ageous phase was basified with 1M NaOH solution and extracted 3 times with DCM. The combined organic layers were dried over MgSO4 and concentrated in vacuo to give the desired product as yellowish oil.

Workup

  1. washwashed twice with water and brine
  2. dry with materialdried over MgSO4
  3. concentrationconcentrated in vacuo
  4. dissolutionThe crude azide was redissolved in 4.3 mL THF
  5. stirringthe mixture was stirred at RT overnight
  6. extractionwas extracted 3 times with Et2O
  7. extractionextracted 3 times with DCM
  8. dry with materialThe combined organic layers were dried over MgSO4
  9. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-eee2ef8039454ec6938a4f4a85ae850f
Source dataset
uspto-grants-2016_08
Patent number
US09409917B2

Reaction notes

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