HuagongsheHuagongshe Chemistry Print Report · For research reference only
(2-Oxo-1,3-oxazolidin-4-yl)methyl 4-methylbenzene-1-sulfonate → (1,3-Oxazolidin-2-on-4-yl)methyl Thioacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (2-Oxo-1,3-oxazolidin-4-yl)methyl 4-methylbenzene-1-sulfonate | HCID 14456891 | — |
| Reactant | HCID 178477078 | HCID 178477078 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | (1,3-Oxazolidin-2-on-4-yl)methyl Thioacetate | HCID 21291365 | 75% |
Reaction Steps
A solution of 2-oxo-1,3-oxazolidin-4-ylmethyl p-toluenesulfonate (1.22 g., 0.0045 mole) and tetrabutylammonium thioacetate (1.71 g, 0.0054 mole) in 75 ml. acetone was refluxed under nitrogen for 90 min. The reaction mixture was concentrated to dryness and the residue was chromatographed on silica gel (250 g). Elution with 4:1 ethyl acetate-hexane yielded 580 mg. of the title compound (75% yield). NMR (CDCl3): 2.38 (s, 3H); 3.06 (d, 2H); 3.84-4.67 (c, 3H); and 6.3 (b, 1H)ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04772597 |
| Source dataset | uspto-grants-1988_09 |
| ORD ID | ord-aed4ffe41a6e4aa181c5b3b60ce684b9 |
| Source note | uspto-grants-1988_09 |