Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 57978641 | HCID 57978641 | — |
| Reactant | HCID 178418416 | HCID 178418416 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Catalyst | Ferrocene-1,1'-bis-(diphenylphosphine) | HCID 635956 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 44447719 | HCID 44447719 | — |
Reaction Steps
To a solution of 2a (280 mg, 0.50 mmol) in DMF (4.8 mL) and methanol (4.8 mL) were added successively palladium (II) acetate (12.0 mg, 0.05 mmol), dppf (54.0 mg, 0.10 mmol) and triethylamine (0.15 mL, 1.10 mmol). The reaction mixture was saturated with carbon monoxide and then heated to 80° C. under a carbon monoxide atmosphere (balloon) for 18 h. After cooling to room temperature, the reaction mixture was poured into water (20 mL) and extracted three times with EtOAc. The combined organic extracts were washed three times with water, dried (MgSO4) and concentrated. Flash chromatography of the residue (silica gel; hexane/EtOAc 9:1) give a solid (122 mg) that was triturated with ether/hexane to provide 2b as a solid (62 mg), m.p. 106-107° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07629467B2 |
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| Source dataset | uspto-grants-2009_12 |
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| ORD ID | ord-7b3213adc280459db7540a005e5b9b67 |
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| Source note | uspto-grants-2009_12 |
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