HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzothiophene 1,1-dioxide → 2,3-Dihydro-1lambda6-benzothiophene-1,1-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzothiophene 1,1-dioxide | HCID 69997 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2,3-Dihydro-1lambda6-benzothiophene-1,1-dione | HCID 284423 | 100% |
Reaction Steps
In a Parr shaker bottle was placed benzo[b]thiophene 1,1-dioxide (5.0 g, 30.08 mmol), palladium on activated carbon (500 mg) and ethanol (100 mL). The bottle was placed on a Parr shaker and charged with 50 psi of hydrogen for 1 h. The reaction mixture was removed from the Parr shaker and filtered through a plug of celite and concentrated in vacuo to afford 2,3-dihydro-benzo[b]thiophene 1,1-dioxide (5.06 g, 100%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07935699B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-40ce3701cd184f03b0d820fbf2c339ff |
| Source note | uspto-grants-2011_05 |