Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | HCID 66591461 | HCID 66591461 | — |
| Reactant | HCID 86618118 | HCID 86618118 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Product | HCID 66591140 | HCID 66591140 | 78% |
Reaction Steps
278 mg (1.20 mmol, 1.5 eq) of methyl 3-(5-bromofuran-2-yl)acrylate and 300 mg (0.80 mmol, 1.0 eq) of octanoylmethyl-[3-(4,4,5,5-tetramethyl[1,3,2]dioxaborolan-2-yl)benzyl]amide (prepared as in 1 e) are dissolved in 5 ml of a 5/1 mixture of dimethylformamide and of 2M potassium phosphate solution. 46 mg (0.04 mmol, 5 mol %) of tetrakis(triphenylphosphine)palladium are added and the reaction mixture is then stirred for 2 hours at 80° C. The reaction is stopped by adding 30 ml of water and is then extracted with ethyl acetate. The organic phases are combined and dried over sodium sulfate. The solvents are evaporated off and the residue is then chromatographed on silica gel (80/20 to 60/40 heptane/ethyl acetate). 250 mg of methyl 3-(5-{3-[(methyloctanoylamino)methyl]phenyl}furan-2-yl)acrylate are obtained. Yield=78%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08129416B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-08a9b6992e0e46f69a2b2d3862c0be42 |
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| Source note | uspto-grants-2012_03 |
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