HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1776192Generated: October 30, 2026
1-Bromo-4-fluorobenzene → HCID 86702136, compound
https://huagongshe.com/reaction/1776192
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Bromo-4-fluorobenzene | HCID 9993 | — |
| Reactant | Benzenamine, 2-chloro-4-fluoro- | HCID 75013 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | 1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine) | HCID 636044 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 86702136 | HCID 86702136 | 68.5% |
Reaction Steps
A round bottom flask was charged with 1-bromo-4-fluorobenzene (6.011 g, 34.4 mmol), 2-chloro-4-fluoroaniline (5.000 g, 34.3 mmol), Xantphos (0.795 g, 1.4 mmol), anhydrous toluene (200 mL), and sodium tert-butoxide (4.952 g, 51.5 mmol). The mixture was degassed and filled with nitrogen, and then tris(dibenzylideneacetone)dipalladium(0) (0.944 g, 1.0 mmol) was added and the reaction was stirred under nitrogen at 100° C. for 16 hrs. After cooling to room temperature, the mixture was filtered through Celite and the filter cake washed with methylene chloride. The filtrate was concentrated and the residue purified by silica gel chromatography (0-20% ethyl acetate/hexanes) to afford a yellowish oil (5.63 g, 68%). 1H NMR (300 MHz, CDCl3) δ 7.14 (dd, 1H, J=8.4, 3.0 Hz), 7.12-6.98 (m, 5H), 6.88 (td, 1H, J=8.7, 3.0 Hz), 5.80 (br s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09265772B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-06e1a9ea411b491da9568dc82ded6430 |
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| Source note | uspto-grants-2016_02 |
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