Sodium Azide → 4-Azidomethyl-2-fluorobenzonitrile
Reaction equation
CS(O[CH2:6][C:7]1[CH:12]=[CH:11][C:10]([C:13]#[N:14])=[C:9]([F:15])[CH:8]=1)(=O)=O.[N-:16]=[N+:17]=[N-:18].[Na+]>O>[N:16]([CH2:6][C:7]1[CH:12]=[CH:11][C:10]([C:13]#[N:14])=[C:9]([F:15])[CH:8]=1)=[N+:17]=[N-:18]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To an ice cooled solution of 4-cyano-3-fluorobenzyl methanesulfonate (1.8 g, 7.9 mmol; see step (iii) above) was added sodium azide (0.80 g, 0.012 mol). The mixture was stirred overnight and then poured into 200 mL of water and extracted three times with diethyl ether. The combined ethereal phase was washed five times with water, dried (Na2SO4) and evaporated. The crude colourless oil could be used without further purification. Yield: 1.2 g (87%).
Workup
- extractionextracted three times with diethyl ether
- washThe combined ethereal phase was washed five times with water
- dry with materialdried (Na2SO4)
- customevaporated
- customThe crude colourless oil could be used without further purification
Sources & evidence
- ORD record
- ord-a9fb1cee57ad428cb44b3b4d0c258bf7
- Source dataset
- uspto-grants-2010_01
- Patent number
- US07645751B2
Reaction notes
Loading…