HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → (2R)-Octan-2-yl 4-(benzyloxy)-3-fluorobenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | (+)-2-Octanol | HCID 2723888 | — |
| Reactant | 4-(Benzyloxy)-3-fluorobenzoic acid | HCID 18757507 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2R)-Octan-2-yl 4-(benzyloxy)-3-fluorobenzoate | HCID 70010782 | — |
Reaction Steps
Triphenylphosphine (7.92 g, 30 mmol) in THF (40 ml) was added dropwise to a stirred solution of compound 11 (7.00 g, 28 mmol), (S)-(+)-octan-2-ol (3.66 g 28 mmol) and diethyl azodicarboxylate (4.87 g, 28 mmol) in THF (100 ml). The reaction solution was left stirring under nitrogen until completion [reaction monitored by TLC (dichloromethane, silica)]. Upon completion, the solvent was removed in vacuo to yield a colourless solid which was purified by column chromatography (dichloromethane) on silica to yield a colourless oil. Yield 10.01 g (99%), [α]D=−22.4° at 25° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06666989B1 |
| Source dataset | uspto-grants-2003_12 |
| ORD ID | ord-b140c9563e51415489f10104a8b8c2d7 |
| Source note | uspto-grants-2003_12 |