HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → HCID 140398709, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | 5-(benzhydryloxy)-2-(hydroxymethyl)-4H-pyran-4-one | HCID 14306387 | — |
| Reactant | HCID 15093893 | HCID 15093893 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 140398709 | HCID 140398709 | 207.6% |
Reaction Steps
To an ice cooled solution of allyl (E)-2-(2-thienyl)-2-(hydroxyimino)acetate (1.0 gm, 4.734 mmol), 5-benzhydryloxy-2-(hydroxymethyl) pyran-4-one (1.46 gm, 4.734 mmol) and triphenylphosphine (1.24 gm, 4.734 mmol) in dry THF (30 ml) under nitrogen was added dropwise diethyl azodicarboxylate (820 μl, 5.208 mmol). The reaction mixture was stirred at room temperature overnight and concentrated under reduced pressure to afford the crude as yellow gum (4.93 gm). The product was purified by silica gel column chromatography using hexane-ethyl acetate (2:1) as eluant to provide the title compound as a gummy foam in 47% yield (1.11 gm).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05888998 |
| Source dataset | uspto-grants-1999_03 |
| ORD ID | ord-7591388962854cca93938c3e132549b9 |
| Source note | uspto-grants-1999_03 |