HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → HCID 21075154, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 21075075 | HCID 21075075 | — |
| Product | HCID 21075154 | HCID 21075154 | 80% |
Reaction Steps
Preparation H6, Step 3: To a soultion of 3-tert-butyl-5-((2-cyanoethyl)carbamoyl)benzoat (520 mg, 1.8 mmol) in MeCN (15 mL) at 0° C. was added NaN3 (117 mg, 1.8 mmol), and Tf20 (0.3 mL, 1.8 mm0l). The mixture was stirred at rt for 16 h before aq NaHCO3 and EtOAc were added. The organic layer was separated and re-washed twice before it was collected, dried over Na2SO4, and concentrated to methyl 3-tert-butyl-5-(2-(2-cyanoethyl)-2H-tetrazol-5-yl)benzoate as an oil (450 mg, 80% yield). MS found: (M+H)+=314.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07163937B2 |
| Source dataset | uspto-grants-2007_01 |
| ORD ID | ord-9afeeca91ce64cf8a720fe3b02ea7692 |
| Source note | uspto-grants-2007_01 |