HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → HCID 73194738, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | 5-(4-Hydroxybenzyl)-3-triphenylmethylthiazolidine-2,4-dione | HCID 2818126 | — |
| Reactant | HCID 54134047 | HCID 54134047 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 73194738 | HCID 73194738 | 40.3% |
Reaction Steps
A solution of 450 mg of diethyl azodicarboxylate in 4 ml of tetrahydrofuran was added dropwise at room temperature to a solution of 383 mg of 2-(benzylideneaminooxy)ethanol (prepared as described in Preparation 1), 1.00 g of 5-(4-hydroxybenzyl)-3-tritylthiazolidine-2,4-dione and 629 mg of triphenylphosphine in 10 ml of tetrahydrofuran, and the resulting mixture was stirred at room temperature for 16 hours. At the end of this time, the reaction product was purified by column chromatography through silica gel, using a 3:1 by volume mixture of hexane and ethyl acetate as the eluent, to give 0.53 g of the title compound as a gum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05780490 |
| Source dataset | uspto-grants-1998_07 |
| ORD ID | ord-75026e21238e4f8f9cbba35c5cf396ef |
| Source note | uspto-grants-1998_07 |