HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → Tert-Butyl 1,2,6-Thiadiazinane-2-Carboxylate 1,1-Dioxide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 23584604 | HCID 23584604 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | Tert-Butyl 1,2,6-Thiadiazinane-2-Carboxylate 1,1-Dioxide | HCID 23583903 | 40% |
Reaction Steps
To a solution of tert-butyl N-(3-chloropropyl)sulfamoylcarbamate (2 g, 7.333 mmol) in DMSO (10 mL), was added K2CO3 (5.068 g, 36.665 mmol) at room temperature. The reaction mixture was agitated for 4 hr and extracted using ethyl acetate and NH4Cl solution. The organic layer was dried over MgSO4. The residue was purified by silica gel column chromatography to give tert-butyl 1,2,6-thiadiazinan-2-carboxylate 1,1-dioxide (689 mg, 2.92 mmol, 40%, white solid). 1H NMR (300 MHz, CDCl3): δ 4.47 (br, 1H), 3.95-3.91 (m, 2H), 3.55-3.49 (m, 2H), 1.89-1.82 (m, 2H), 1.54 (m, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09073906B2 |
| Source dataset | uspto-grants-2015_07 |
| ORD ID | ord-c4b6b1ef80924fce92eb1f022df06b9f |
| Source note | uspto-grants-2015_07 |