HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hexane → 4-(3-Furyl)-7-methylcoumarin
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Trimethyl borate | HCID 8470 | — |
| Reactant | 3-Bromofuran | HCID 89164 | — |
| Reactant | 7-Methyl-2-oxo-2H-chromen-4-YL trifluoromethanesulfonate | HCID 23370238 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-(3-Furyl)-7-methylcoumarin | HCID 23370190 | — |
Reaction Steps
To a solution of 3-bromofuran (1.9 g, 12.7 mmol) in dry ET2O (30 mL) at -70° C. was added BuLi in hexane (1.9M, 6.7 mL, 12.7 mmol) and the resulting mixture was stirred for 20 min.. Trimethyl borate (Aldrich) (1.4 mL, 12.7 mmol) was added dropwise and the mixture stirred for 20 min.. A solution of the triflate from Step 4 in THF: H2O (24 mL: 6 mL) containing (Ph3P)4Pd (1.1 g, 0.97 mmol) was added and the reaction was heated to reflux for 16 h. The reaction mixture was cooled to r.t. and EtOAc was added and the organic phase washed with H2O (3×), brine, dried over MgSO4 and evaporated to give a white solid. A swish in EtOAc gave after filtration 1.8 g (82%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05552437 |
| Source dataset | uspto-grants-1996_09 |
| ORD ID | ord-e8a040c739b041babc0aa3b9ed3d30cc |
| Source note | uspto-grants-1996_09 |