HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Dibromopropane → 1,3-Bis(4-fluoro-2-iodophenoxy)propane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Dibromopropane | HCID 8001 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Fluoro-2-iodophenol | HCID 10171417 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 1,3-Bis(4-fluoro-2-iodophenoxy)propane | HCID 66780595 | — |
Reaction Steps
To a solution of 15.00 g (63.03 mmol) of 4-fluoro-2-iodophenol (P7), Preparation 7 and 6.40 g (31.68 mmol) of 1,3-dibromopropane in 200 mL of acetone add 26.00 g (188.4 mmol) of potassium carbonate. Reflux the resulting reaction mixture for 24 hours. Cool the reaction mixture to room temperature, filter it, and concentrate the filtrate by rotary evaporation. Crystallize the resulting solid from acetonitrile to yield 12.00 g (74%) of (P8) as a white crystalline solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09029487B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-d97b5df56a5a4d84ba81625083555a2a |
| Source note | uspto-grants-2015_05 |