HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → HCID 86709277, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 86709276 | HCID 86709276 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86709277 | HCID 86709277 | 84% |
Reaction Steps
To a solution of N-(2-((Tert-butyldimethylsilyl)oxy)ethyl)-1-phenylethenesulfonamide (717 mg, 2.1 mmol) in tetrahydrofuran (7 mL) at 0° C. was added tetrabutylammonium fluoride (1.0 M in THF) (2.2 mL, 2.2 mmol) dropwise and the reaction was stirred at room temperature for 16 hours. Saturated NH4Cl was then added and the product was extracted with dichloromethane (×2), dried with MgSO4, concentrated and purified by silica gel column chromatography (0-100% EtOAc in heptane) to give 3-phenyl-1,4,5-oxathiazepane 4,4-dioxide (401 mg, 84% yield). (24 g, 70% yield). LCMS (ESI), m/z, 228. [M+H]+. (Reference: P. Hansen, et al. Org. Lett. 2008, 2951).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09115101B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-96469ba0f4cb44f78c32a1bf1f1148d9 |
| Source note | uspto-grants-2015_08 |