HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → S-(1-(4,5-dihydrothiazol-2-yl)azetidin-3-yl) ethanethioate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diethyl azodicarboxylate | HCID 5462977 | — |
| Reactant | 1-(4,5-Dihydrothiazol-2-yl)azetidin-3-ol | HCID 10986515 | — |
| Reactant | HCID 178418634 | HCID 178418634 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | S-(1-(4,5-dihydrothiazol-2-yl)azetidin-3-yl) ethanethioate | HCID 11790619 | 65% |
Reaction Steps
There were added 119 mg of 3-hydroxy-1-(1,3-thiazolin-2-yl)azetidine (6) and two molar equivalents of thioacetic acid, while cooled with ice, to 10 ml of tetrahydrofuran solution containing two molar equivalents of triphenylphosphine and two molar equivalents of diethylazodicarboxylate, and the resultant solution was stirred for one hour at the same temperature, and for further one hour at a room temperature. The solvent of the reaction liquid was evaporated in a vacuum, and the obtained residue was subjected to silica gel column chromatography (eluent: chloroform-ethanol), and, thus, there was obtained 107 mg (yield: 65%) of 3-acetylthio-1-(1,3-thiazolin-2-yl)azetidine (7).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05659043 |
| Source dataset | uspto-grants-1997_08 |
| ORD ID | ord-75aa402e56ea4304993e1a1a5a7b8475 |
| Source note | uspto-grants-1997_08 |