HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 628574Generated: October 27, 2026
4-Bromo-2-fluoro-1-nitrobenzene → HCID 86661419, compound
https://huagongshe.com/reaction/628574
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Bromo-2-fluoro-1-nitrobenzene | HCID 2783362 | — |
| Reactant | 2-Nitro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline | HCID 16217914 | — |
| Solvent | Water 1,2-dimethoxyethane | HCID 18180031 | — |
| Product | HCID 86661419 | HCID 86661419 | 45.3% |
Reaction Steps
4-Bromo-2-fluoro-1-nitrobenzene (500 mg, 2.27 mmol), 2-nitro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline (660 mg, 2.50 mmol) and K2CO2 (940 mg, 6.81 mmol) were suspended in DME-H2O (4:1, 15 mL) and purged with nitrogen. The solution was degassed by sonication before Pd(dppf)Cl2 (185 mg, 10 mol %) was added. The mixture was heated to 130° C. for 10 min under microwave irradiation. The cooled mixture was partitioned between EtOAc and H2O. The aqueous layer was extracted with EtOAc (2×50 mL). The combined organic extracts were washed with brine, dried (MgSO4), filtered and concentrated. The resulting black solid was absorbed onto silica and purified by column chromatography (4:1 to 1:1 petrol-EtOAc) to give the product as an orange solid (285 mg, 45%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09314456B2 |
|---|
| Source dataset | uspto-grants-2016_04 |
|---|
| ORD ID | ord-02edcea09dea4c84ae3cf49ac2ec0851 |
|---|
| Source note | uspto-grants-2016_04 |
|---|