HuagongsheHuagongshe Chemistry Print Report · For research reference only
P-Toluenesulfonamide → 6-Tosyl-2-oxa-6-azaspiro[3.3]heptane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | P-Toluenesulfonamide | HCID 6269 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Pentaerythritol tribromide | HCID 15206 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 6-Tosyl-2-oxa-6-azaspiro[3.3]heptane | HCID 23319891 | 63% |
Reaction Steps
To a solution of 3-bromo-2,2-bis(bromomethyl)propanol (127) (3.25 g, 10 mmol) and potassium hydroxide (1.12 g, 20 mmol, in 10 mL water) in EtOH (20 mL) were added toluene-4-sulfonamide (3.76 g, 22 mmol). The reaction mixture was refluxed for 2 h, evaporated to remove EtOH then diluted with EAOAc (20 mL), washed with H2O (20 mL). The organic layer was washed with brine (20 mL), dried over Na2SO4, and filtered, evaporated to give the product to give 6-(toluene-4-sulfonyl)-2-oxa-6-aza-spiro[3.3]heptane (128) (1.6 g, 6.3 mmol, yield: 63%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08957073B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-9a27ba83252e4f7291dd076301e982ea |
| Source note | uspto-grants-2015_02 |