HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 4-Amino-3-bromo-2,5-difluorobenzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 4-Amino-2,5-difluorobenzonitrile | HCID 2735900 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 4-Amino-3-bromo-2,5-difluorobenzonitrile | HCID 14621019 | 71% |
Reaction Steps
A mixture of 1.65 mL of Br2, 2 mL of H2O and 5 g of 4-amino-2,5-difluorobenzonitrile in 50 mL of AcOH is stirred at 20°-25° for 16 hours. The solvents are removed in vacuo and the residue partitioned between 100 mL of H2O and 3×200 ml of CH2Cl2. The CH2Cl2 extracts are washed with H2O, saturated NaHCO3, H2O (100 mL each), dried with Na2SO4 and evaporated in vacuo to give 6.89 g of crude 4-amino-3-bromo-2,5-difluorobenzonitrile. This is purified by dry-column chromatography using SiO2 to give 5.38 g (71% yield). Recrystallization from CH2Cl2 /hexane affords analytically pure material, m.p. 106°-108° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04863959 |
| Source dataset | uspto-grants-1989_09 |
| ORD ID | ord-690245e71855466eb051ecc7f75c2a27 |
| Source note | uspto-grants-1989_09 |