HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetamide → HCID 59167767, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetamide | HCID 178 | — |
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | Octanedioic acid methyl ester 2-oxo-2-phenylethyl ester | HCID 59167744 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | HCID 59167767 | HCID 59167767 | 88% |
Reaction Steps
Heat a mixture of octanedioic acid methyl ester 2-oxo-2-phenylethyl ester (6.93 g, 22.6 mmol), acetamide (6.75 g, 114 mmol) and boron trifluoride diethyl etherate (3.0 mL, 23.7 mmol) at 135-140° C. under nitrogen for 4 hours. Cool the mixture, dilute with saturated NaHCO3 solution (100 mL), and extract with ethyl acetate (250 mL). Wash the organic extract with 100 mL of saturated aqueous sodium chloride (brine) and dry over sodium sulfate. Remove the solvent under reduced pressure and purify the residue by flash column chromatography on silica gel, eluting with hexanes/ethyl acetate (85:15), to provide 7-(4-phenyloxazol-2-yl)heptanoic acid methyl ester (5.7 g, 88%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08552039B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-16877312d4d44af1bb2ba2e843db7d51 |
| Source note | uspto-grants-2013_10 |