HuagongsheHuagongshe Chemistry Print Report · For research reference only
m-Chloroperbenzoic acid → 2-[2-(2-Azido-Ethoxy)-Ethylsulfonyl]-Ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Reactant | 2-(2-Azidoethoxy)ethyl 4-methylbenzenesulfonate | HCID 60020448 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-[2-(2-Azido-Ethoxy)-Ethylsulfonyl]-Ethanol | HCID 86670300 | 86% |
Reaction Steps
A solution of sulfide 3 (8.41 g, 44 mmol) in CH2Cl2 (100 ml) was cooled in an ice bath. mCPBA (84% purity, 27.1 g, 3 equiv.) was added portion wise and the resulting solution was stirred at RT for 16 h. An aqueous 1 M NaHSO3 solution (20 ml) was added, and the resulting suspension was vigorously stirred at RT for 30 min. The white m-chlorobenzoic acid precipitate was filtrated over a celite pad. The organic layer was washed with a saturated aqueous NaHCO3 solution (3×20 ml), dried over MgSO4, filtrated then concentrated under reduced pressure. Purification by flash column chromatography (eluent: pet. ether/AcOEt 1:1 then 3:7 then pure AcOEt) afforded sulfone 5 as a colorless liquid (8.41 g, 86%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09073969B2 |
| Source dataset | uspto-grants-2015_07 |
| ORD ID | ord-767355a929014f99b4acdf5067211717 |
| Source note | uspto-grants-2015_07 |