HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → 4-Chloro-1-[2-chloro-4-(3,5-difluorophenoxy)phenoxy]methylbenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 4-Chlorobenzyl alcohol | HCID 13397 | — |
| Reactant | 2-Chloro-4-(3,5-difluorophenoxy)phenol | HCID 19792252 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Chloro-1-[2-chloro-4-(3,5-difluorophenoxy)phenoxy]methylbenzene | HCID 19792248 | 61.7% |
Reaction Steps
A mixture of 0.95 g of 2-chloro-4-(3,5-difluorophenoxy)phenol, 0.54 g of p-chlorobenzyl alcohol, 1.01 g of triphenylphosphine, 0.65 g of diethylazadicarboxylate and 90 ml of tetrahydrofuran was stirred at room temperature. After 48 hours, the reaction mixture was concentrated, and 50 ml of diethyl ether was added thereto. The precipitate were removed by filtration, and the filtrate was concentrated. The residue was subjected to silica gel chromatography to give 0.87 g of 4-chloro-1-[2-chloro-4-(3,5-difluorophenoxy)phenoxy]methylbenzene. Yield, 62%. m.p.: 95.3° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05250574 |
| Source dataset | uspto-grants-1993_10 |
| ORD ID | ord-29766aecf7e6468c85271bb2e7a663ab |
| Source note | uspto-grants-1993_10 |