HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diphenyl sulfide → HCID 24898113, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diphenyl sulfide | HCID 8766 | — |
| Reactant | HCID 59300603 | HCID 59300603 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 24898113 | HCID 24898113 | — |
Reaction Steps
To a suspension of Pd/C (20.0 mg, 10%) with Ph2S (1.0%) in MeOH (5.0 mL), was added 20 (25.0 mg, 0.164 mmol) in MeOH (1.0 mL). The reaction mixture was purged with hydrogen three times. The mixture was then stirred under hydrogen at room temperature overnight. The catalyst was filtered off, and the solvent was evaporated to give the title compound 23. 1H NMR (CD3CN) δ 1.55-2.02 (m, 8H), 2.93 (dd, J=7.3, 16.4 Hz, 1H), 3.16 (dd, J=7.3, 16.4 Hz, 1H), 3.33 (m, 1H), 4.53 (m, 1H), 5.05 (s, 2H), 6.24 (d, J=1.7 Hz, 1H), 6.94 (d, J=6.6 Hz, 2H), 7.22-7.26 (m, 4H), 7.49 (d, J=5.0 Hz, 1H), 8.45 (d, J=1.7 Hz, 1H). MS ESI (pos.) m/e: 476 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07714008B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-218e077e79a945e98ed879a250434dc1 |
| Source note | uspto-grants-2010_05 |