HuagongsheHuagongshe Chemistry Print Report · For research reference only
4,5-Dihydro-2-(methylthio)thiazole → 1-(4,5-Dihydrothiazol-2-yl)azetidin-3-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4,5-Dihydro-2-(methylthio)thiazole | HCID 88324 | — |
| Reactant | 3-Hydroxyazetidine hydrochloride | HCID 2759290 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(4,5-Dihydrothiazol-2-yl)azetidin-3-ol | HCID 10986515 | 81.5% |
Reaction Steps
To a solution of 109 mg of 3-hydroxyazetidine HCl [Compound (15)] in 5 ml of ethanol was added a mixture of 133 mg of 2-methylthiothiazoline [Compound (16)] and sodium methoxide (0.9 equivalent mole), and the reaction mixture was refluxed for 8 hours. After removal of the solvent under reduced pressure, the resulting residue was dissolved in chloroform and washed with saturated saline solution. After removal of the solvent under reduced pressure, the resulting residue was washed with diethylether to give 119 mg (81.5%) of 3-hydroxy-1-(thiazolin-2-yl)azetidine [Compound (17)] as crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05886172 |
| Source dataset | uspto-grants-1999_03 |
| ORD ID | ord-4ac4a670b0e74c919204719ffebfd63a |
| Source note | uspto-grants-1999_03 |