HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2192889Generated: October 26, 2026
Sodium Sulfite → ethyl 2-[3-bromo-4-(cyclopropylsulfonyl)phenyl]-3-(tetrahydro-2H-pyran-4-yl)acrylate
https://huagongshe.com/reaction/2192889
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | ethyl 2-[3-bromo-4-(cyclopropylsulfanyl)phenyl]-3-(tetrahydro-2H-pyran-4-yl)acrylate | HCID 68671827 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | ethyl 2-[3-bromo-4-(cyclopropylsulfonyl)phenyl]-3-(tetrahydro-2H-pyran-4-yl)acrylate | HCID 68671424 | — |
Reaction Steps
Ethyl 2-[3-bromo-4-(cyclopropylsulfanyl)phenyl]-3-(tetrahydro-2H-pyran-4-yl)acrylate (4.57 g) was dissolved in dichloromethane (91 mL), followed by ice-cooling. To this solution was added m-chloroperbenzoic acid (5.75 g) in 5 divided portions. It was warmed to room temperature, followed by stirring for 2 hours. To the reaction mixture was added a saturated aqueous sodium hydrogen carbonate solution, and further added a 1 M aqueous sodium sulfite solution. The organic layer was separated and the aqueous layer was then extracted with dichloromethane. The organic layer was further washed with a saturated aqueous sodium hydrogen carbonate solution, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure to obtain ethyl 2-[3-bromo-4-(cyclopropylsulfonyl)phenyl]-3-(tetrahydro-2H-pyran-4-yl)acrylate (4.72 g) as an (E)/(Z)-mixture.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08329707B2 |
|---|
| Source dataset | uspto-grants-2012_12 |
|---|
| ORD ID | ord-ec4afa313bfe4581b651e74d3c503d12 |
|---|
| Source note | uspto-grants-2012_12 |
|---|