HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2421582Generated: November 2, 2026
Bromine → 1,2-Dibromo-4,5-diethoxy-3-fluorobenzene
https://huagongshe.com/reaction/2421582
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 5-Bromo-1,2-diethoxy-3-fluorobenzene | HCID 59668392 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1,2-Dibromo-4,5-diethoxy-3-fluorobenzene | HCID 11709889 | 101.4% |
Reaction Steps
To a solution of 5-bromo-1,2-diethoxy-3-fluorobenzene (40.0 g, 0.15 mol) in acetic acid (200 mL), sodium acetate (16.2 g, 0.20 mol) and bromine (31.6 g, 0.20 mol) were added sequentially at room temperature, and the mixture was stirred at 50° C. for 1.5 hours. The reaction mixture was cooled to room temperature, and a saturated aqueous solution of sodium thiosulfate (400 mL) and water (400 mL) were added sequentially. The mixture was extracted once with heptane (800 mL) and three times with heptane (400 mL). The organic layer was washed sequentially with water (400 mL), once with a 2 N aqueous solution of sodium hydroxide (200 mL), once with a 2 N aqueous solution of sodium hydroxide (100 mL), and water (400 mL), then dried over anhydrous magnesium sulfate. The solvent was distilled off from the organic layer under reduced pressure and the residue was filtered. The filtrate was then purified by silica gel column chromatography (hexane, ethyl acetate) to give 52.0 g of the title compound (yield:quant.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07956222B2 |
|---|
| Source dataset | uspto-grants-2011_06 |
|---|
| ORD ID | ord-7633cd7d9e024e218a460e833c48e025 |
|---|
| Source note | uspto-grants-2011_06 |
|---|