HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Hexaethylene Glycol Di-p-toluenesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Hexaethylene Glycol | HCID 17472 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | Hexaethylene Glycol Di-p-toluenesulfonate | HCID 428918 | — |
Reaction Steps
To a solution of 1.48 g (5.24 mmol) of hexaethylene glycol in dry pyridine (30 ml) was added 2.19 g (11.5 mmol) of p-toluenesulfonyl chloride in an atmosphere of argon, and the mixture was allowed to react at room temperature for 15 hours. To the solution was added water followed by addition of conc. hydrochloric acid to adjust the pH to 4, and the resulting mixture was extracted with ethyl acetate. The organic layer was washed with water and then concentrated under reduced pressure. The residue thus obtained was subjected to silica gel column chromatography for separation and purification. Elution with dichloromethane-methanol (100:1) yielded 2.85 g (4.82 mmol) of O,O'-ditosyl-3,6,9,12,15-pentaoxaheptadecane-1,17-diol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05043142 |
| Source dataset | uspto-grants-1991_08 |
| ORD ID | ord-e05a66d2ed6849f298150f845352fe87 |
| Source note | uspto-grants-1991_08 |