Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | HCID 10223945 | HCID 10223945 | — |
| Catalyst | Ferrocene-1,1'-bis-(diphenylphosphine) | HCID 635956 | — |
| Catalyst | Tris(dibenzylideneacetone) dipalladium | HCID 9832798 | — |
| Product | HCID 10292411 | HCID 10292411 | — |
Reaction Steps
The final product of STEP 4, EXAMPLE 13 (500 mg) was dissolved in DMF (10 ml) and water (1.0 ml) and was treated with tris(dibenzylideneacetone) dipalladium(0) (51 mg) and bis(diphenylphosphino)ferrocene (75 mg).The reaction mixture was heated to reflux and was allowed to reflux for 20 hours under nitrogen atmosphere. The mixture was cooled to room temperature and was filtered through celite under vacuum. The filtrate was concentrated. The residue was dissolved in ethyl acetate and was washed with a saturated solution of ammonium chloride and dried over Na2SO4. The solid was filtered and the filtrate was concentrated. The cude product was purified by flash chromatography on silica gel (EA/Hexane/NH4OH:80/19.5/0.5) to give 181 mg of desired compound as oily gum. NMR spectrum was consistent for the proposed structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06531494B1 |
|---|
| Source dataset | uspto-grants-2003_03 |
|---|
| ORD ID | ord-04c4523118434baaaf079dc5f4c7004e |
|---|
| Source note | uspto-grants-2003_03 |
|---|