HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl Sulfoxide → HCID 67158730, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 76647763 | HCID 76647763 | — |
| Reactant | HCID 178418416 | HCID 178418416 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Catalyst | Ferrocene-1,1'-bis-(diphenylphosphine) | HCID 635956 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 67158730 | HCID 67158730 | — |
Reaction Steps
Treat a mixture containing trifluoromethanesulfonic acid 6-(1-ethylpropenyl)naphthalen-2-yl ester (0.92 g, 2.67 mmol), Pd(OAc)2 (0.020 mg, 0.09 mmol), bis-(diphenylphosphino)ferrocene (0.046 g, 0.083 mmol), Et3N (0.67 mL, 4.81 mmol), in MeOH (10 mL) and DMSO (15 mL) with carbon monoxide at 100 psi at 80° C. for 4 h. Pour the reaction mixture into ether (100 mL) and wash the mixture with brine (4×50 mL). Dilute the organic layer with EtOAc (100 mL), wash with brine, then dry over Na2SO4 and filter. Concentrate the filtrate to give the title compound as an off-white solid (0.67 g, quant). MS (ES) in/e 255 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07943795B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-c1eaff9626344ac1aad21f1c0eedc939 |
| Source note | uspto-grants-2011_05 |