HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 3-Bromo-2-chloro-6-fluorobenzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| Reactant | 3-Bromo-2-chloro-6-fluorobenzamide | HCID 71239503 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Bromo-2-chloro-6-fluorobenzonitrile | HCID 71239391 | — |
Reaction Steps
To a solution of 3-bromo-2-chloro-6-fluorobenzamide (3.56 mmol) in 50 mL DCM were added 1.5 mL Et3N followed by trifluoromethanesulfonic acid anhydride (7.11 mmol) at 0° C. The ice bath was removed and the reaction mixture was stirred at RT. After 30 min, water was added and the mixture was extracted with DCM (3×). The combined organic layers were dried over MgSO4 and concentrated in vacuo to obtain the desired compound as brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09221832B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-0417eee7762a4333be31dc3b00dc285b |
| Source note | uspto-grants-2015_12 |