HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 89586109, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Acetone | HCID 180 | — |
| Reactant | Ethyl 3-bromofuran-2-carboxylate | HCID 22456149 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 89586109 | HCID 89586109 | — |
Reaction Steps
To a solution of ethyl 3-bromofuran-2-carboxylate (16.2 g) and acetone (5.14 mL) in toluene (250 mL) was added potassium tert-butoxide (15.7 g) at 0° C. portionwise. The reaction mixture was stirred at room temperature for 2 hr, and acetic acid (8.01 mL) and water (250 mL) were added. The organic layer was separated, washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) and recrystallized from hexane/ethyl acetate to give the title compound (10.9 g, enol/diketone=88/12).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09150588B2 |
| Source dataset | uspto-grants-2015_10 |
| ORD ID | ord-6d49d26bef7140a48a6da7c6f841c264 |
| Source note | uspto-grants-2015_10 |