HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Carbonate → HCID 18947034, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | HCID 18947041 | HCID 18947041 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 18947034 | HCID 18947034 | 34.4% |
Reaction Steps
0.91 g (7.5 mmol) of phenylboronic acid, 0.209 g (0.38 mmol) of (dibenzylideneacetone)-palladium(O), 0,397 g (1.5 mmol) of triphenylphosphine and 7.5 ml (15 mmol) of a 2M sodium carbonate solution are added to a solution of 3.2 g (8.3 mmol) of 1,3-dibromo-5-(1,1-dimethylethoxy)carbonyl-5,6-dihydro-4H-thieno[3,4-c]pyrrole in 45 ml of toluene. The mixture is heated at reflux for 5.5 hours and then cooled. The organic phase is separated by settling, washed with water, dried over magnesium sulphate and then evaporated to dryness. The residue is purified by chromatography on silica gel using the 5/95 ethyl acetate/hexane eluent mixture. There is obtained 0.98 g of a white solid. Yield 34%. Melting point: 139°-140° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05380742 |
| Source dataset | uspto-grants-1995_01 |
| ORD ID | ord-d7bf7d83b83143b3bec8bb6011341012 |
| Source note | uspto-grants-1995_01 |