HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → 4-[2-(4-Bromo-3-fluorophenoxy)ethyl]morpholine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2-Morpholinoethanol | HCID 61163 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Reactant | 4-Bromo-3-fluorophenol | HCID 2779153 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-[2-(4-Bromo-3-fluorophenoxy)ethyl]morpholine | HCID 59000729 | 33% |
Reaction Steps
A flask was charged with 4-bromo-3-fluorophenol (4.999 g, 26.2 mmol) and triphenylphosphine (10.298 g, 39.3 mmol). Methylene chloride (120 mL) was added followed by 2-morpholinoethanol (4 mL, 33.0 mmol) and the solution was stirred on an ice water bath to cool. After 5 minutes, diisopropyl azodicarboxylate (7.6 ml, 39.1 mmol) was added over 6 to 8 minutes. The reaction was left stirring on the cold bath to slowly warm to room temperature overnight. The reaction was concentrated and the residue purified by flash chromatography (25% to 100% EtOAc in hexanes) to provide the product as a colorless oil (2.621 g, 33%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07968574B2 |
| Source dataset | uspto-grants-2011_06 |
| ORD ID | ord-6c6846fff8fb4b318007952b9dfff9af |
| Source note | uspto-grants-2011_06 |