HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 6-Benzenesulfonyl-1,2,3,4-tetrahydro-naphthalene-1-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 6-Benzenesulfonyl-3,4-dihydro-naphthalene-1-carbonitrile | HCID 59021756 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 6-Benzenesulfonyl-1,2,3,4-tetrahydro-naphthalene-1-carbonitrile | HCID 59021749 | 90.1% |
Reaction Steps
6-Benzenesulfonyl-3,4-dihydro-naphthalene-1-carbonitrile (5.1 g, 17.2 mmol), 70 mL EtOH, and 50 mL acetic acid were placed in a Parr vessel, and 1.0 g of 10% Palladium on carbon (Fluka Chemica Co.) was added. The reaction mixture was shaken for 15 hours under 55 psi hydrogen. The Parr vessel was purged with nitrogen and the reaction mixture was filtered. The filtrate was added to 500 mL water, and the aqueous mixture was extracted twice with 200 mL of EtOAc. The combined organic layers were dried (MgSO4) and evaporated to yield 4.6 g (15.5 mmol, 90%) of 6-benzenesulfonyl-1,2,3,4-tetrahydro-naphthalene-1-carbonitrile as an oil. MS: 298 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08889906B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-2de491ac4047468eb5ba0f8a507723f7 |
| Source note | uspto-grants-2014_11 |