Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Butylamine | HCID 8007 | — |
| Reactant | Tributyl borate | HCID 12712 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Boron trioxide | HCID 518682 | — |
| Reactant | 4-Hydroxy-2-Methoxybenzaldehyde | HCID 519541 | — |
| Reactant | 6-(4-Hydroxyphenyl)-2,4-hexanedione | HCID 59748562 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | HCID 68554935 | HCID 68554935 | 44% |
Reaction Steps
6-(4-Hydroxyphenyl)hexane-2,4-dione (18 mg, 87 μmol) and boron trioxide (22 mg, 0.32 mmol) was placed in a 20 mL reaction vessel, and dissolved in 0.4 mL of ethyl acetate. To the stirring solution at 80° C. were added 4-hydroxy-2-methoxybenzaldehyde (12 mg, 78 μmol) and tri-n-butyl borate (50 μL, 0.19 mmol). After the reaction mixture was stirred for 2 h at the same temperature, n-butylamine (19 μL, 0.19 mmol) was added with additional stirring for 1 h. The reaction mixture was treated with a 1:1 solution (1 mL) of 1N HCl and brine, and was stirred at 50° C. for 5 min to 1 h (if necessary, the reaction mixture was neutralized by saturated NaHCO3 aqueous solution). The organic layer was purified directly by silica gel column chromatography (eluting with hexane/ethyl acetate or chloroform/methanol) to obtain the title compound as a solid (11.6 mg, 44%) having the following characteristics.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08962674B2 |
|---|
| Source dataset | uspto-grants-2015_02 |
|---|
| ORD ID | ord-40760a8e18ac4bbaab320bb57fd052cf |
|---|
| Source note | uspto-grants-2015_02 |
|---|