HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 508411Generated: November 4, 2026
3,4-Dichlorophenol → 1-Bromo-5-chloro-4-((3,4-dichlorophenoxy)methyl)-2-fluorobenzene
https://huagongshe.com/reaction/508411
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3,4-Dichlorophenol | HCID 7258 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Bromo-4-(bromomethyl)-5-chloro-2-fluorobenzene | HCID 66666755 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-Bromo-5-chloro-4-((3,4-dichlorophenoxy)methyl)-2-fluorobenzene | HCID 66666443 | 110.3% |
Reaction Steps
A mixture of 3,4 dichlorophenol (730 mg, 4.48 mmol), 1-bromo-4-(bromomethyl)-5-chloro-2-fluorobenzene (Preparation 2, 1.35 g, 4.48 mmol), and potassium carbonate (1.87 g, 13.5 mmol) in acetone (56 mL) was stirred for 72 hours at room temperature under a nitrogen atmosphere. The reaction mixture was diluted with ethyl acetate (100 mL) and filtered through Arbocel™. The Arbocel™ was washed with ethyl acetate (2×50 mL) and the combined organic extracts were concentrated in vacuo to afford a pale yellow solid. The solid was then dissolved in ethyl acetate (150 mL) and washed successively with aqueous sodium hydroxide solution (0.5 M, 100 mL), brine (3×100 mL), dried over sodium sulphate, filtered and concentrated in vacuo to afford an off white solid (1.90 g). Recrystallisation from hot heptane afforded the title compound (920 mg, 53%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09096500B2 |
|---|
| Source dataset | uspto-grants-2015_08 |
|---|
| ORD ID | ord-0e3d6a6b7af0435d983cec2a67a28a03 |
|---|
| Source note | uspto-grants-2015_08 |
|---|