HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → HCID 18620468, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | 2-(Trifluoromethylsulfanyl)ethanol | HCID 4089698 | — |
| Reactant | HCID 178429419 | HCID 178429419 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl acetate pentane | HCID 22335286 | — |
| Product | HCID 18620468 | HCID 18620468 | 55.7% |
Reaction Steps
A mixture of 1A (0.55 g), 2-(trifluoromethylthio)-ethanol (0.35 g, Example A), triphenylphosphine (0.64 g) and diethyl azodicarboxylate (0.42 g) in dry tetrahydrofuran (5 ml) is stirred for 20 hours at ambient temperature. The reaction mixture is diluted with pentane/ethyl acetate (by volume ration 1/1) and filtered through a bed of silica gel. The filtrate is washed with water. The organic layer is dried with anhydrous magnesium sulfate, filtered and evaporated in vacuo. Purification by flash chromatography (silica gel: pentane/ethyl acetate 9/1 v/v) yields 0.45 g of the title compound as an colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06534447B1 |
| Source dataset | uspto-grants-2003_03 |
| ORD ID | ord-fad1989119e94b57b3eb3c7f9657511f |
| Source note | uspto-grants-2003_03 |