HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → Methyl 4-[(2-phenoxyphenyl)methoxy]benzeneacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | Benzeneacetic acid, 4-hydroxy-, methyl ester | HCID 518900 | — |
| Reactant | 2-Phenoxybenzyl alcohol | HCID 3660111 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 4-[(2-phenoxyphenyl)methoxy]benzeneacetate | HCID 131730197 | — |
Reaction Steps
To a solution of (2-phenoxyphenyl)methanol (1.43 g) in tetrahydrofuran (25 ml), 1.19 g of methyl(4-hydroxyphenyl)acetate, 2.82 g of triphenylphosphine, and 4.86 ml of diethyl azodicarboxylate (45% toluene solution) were added, and the reaction solution was stirred at room temperature for 30 minutes. The reaction solvent was distilled off under reduced pressure, and the residue obtained was purified by silica gel column chromatography (eluent: ethyl acetate/hexane (5:95-30:70)) to afford the title compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08367708B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-4047015b89544303a7efc9d35252450d |
| Source note | uspto-grants-2013_02 |