HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 7-(1,3-Dioxoisoindol-2-yl)heptyl-4-methylbenzenesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | 2-(7-Hydroxyheptyl)isoindoline-1,3-dione | HCID 18970904 | — |
| Solvent | Water | HCID 962 | — |
| Product | 7-(1,3-Dioxoisoindol-2-yl)heptyl-4-methylbenzenesulfonate | HCID 86762180 | — |
Reaction Steps
783 mg of 2-(7-hydroxyheptyl)isoindol-1,3-dione was added to 40 mL of DCM, and 800 mg of p-toluenesulfonyl chloride was added. Pyridine was then added dropwise with stirring, and the mixture was stirred overnight. After 24 h, 100 mL of water was added to the reaction system, which was then violently vibrated and isolated. The water layer was extracted with 50 mL of DCM. The organic layers were combined, successively washed with 100 mL of 5% citric acid aqueous solution, 100 mL of saturated sodium carbonate aqueous solution, and 100 mL of saturated sodium chloride aqueous solution, dried over 5 g of MgSO4 for 30 min, and concentrated via a rotary evaporator to obtain an oily liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08604065B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-b637c823c2ff413faab16203db951f4c |
| Source note | uspto-grants-2013_12 |