HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Dibromopropane → 1,3-Bis(2,4-difluoro-6-iodophenoxy)propane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Dibromopropane | HCID 8001 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,4-Difluoro-6-iodophenol | HCID 22221624 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 1,3-Bis(2,4-difluoro-6-iodophenoxy)propane | HCID 58516556 | — |
Reaction Steps
To a solution of 7.68 g (30 mmol) of 2,4-difluoro-6-iodophenol (P7), Preparation 7 and 3.03 g (15 mmol) of 1,3-dibromopropane in 125 mL of acetone add 12.42 g (90 mmol) of potassium carbonate. Reflux the resulting reaction mixture for 48 hours. Cool the reaction mixture to room temperature, filter it, and extract the resulting filtrate thoroughly with methylene chloride. Combine methylene chloride extracts and concentrate them by rotary evaporation. Crystallize the resulting solid from hexanes to yield 3.4 g (41.1%) of (P8) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09000108B2 |
| Source dataset | uspto-grants-2015_04 |
| ORD ID | ord-6902d52c34c04724a6c1cfadea210f36 |
| Source note | uspto-grants-2015_04 |