HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Azide → 4-(2-Azidoacetyl)benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | 4-(Bromoacetyl)benzonitrile | HCID 98654 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-(2-Azidoacetyl)benzonitrile | HCID 58661729 | 94% |
Reaction Steps
To a solution of the commercially available 4-bromoacetyl-benzonitrile (5 g, 22.32 mmol) in 150 mL of methanol was added sodium azide (1.74 g, 26.78 mmol) and the contents stirred at room temperature for 2 h. After removal of the solvent, the residue was treated with water (50 mL) and extracted with dichloromethane (3×50 mL). The combined organic layers were dried over MgSO4 and concentrated to give a yellow solid (3.90 g, 94%). This compound was used for the next step without any further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08658659B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-b2c5886bde8446999e9f1ed768a4f001 |
| Source note | uspto-grants-2014_02 |