Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | HCID 66591357 | HCID 66591357 | — |
| Reactant | HCID 86618120 | HCID 86618120 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Product | HCID 66591532 | HCID 66591532 | 65% |
Reaction Steps
300 mg (0.90 mmol, 1.0 eq) of octanoyl(4-bromothiophen-2-ylmethyl)methylamide and 326 mg (1.08 mmol, 1.2 eq) of ethyl 3-[4-(4,4,5,5-tetramethyl[1,3,2]dioxaborolan-2-yl)phenyl]acrylate are dissolved in 4 ml of a 5/1 mixture of dimethylformamide and of 2M potassium phosphate solution. 52 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 ethyl 3-(4-{5-[(methyloctanoylamino)methyl]thiophen-3-yl}phenyl)acrylate are obtained. Yield=65%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08129416B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-fa3ab75ef1394c4d8c3d945178c1df98 |
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| Source note | uspto-grants-2012_03 |
|---|