HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl Benzoate → HCID 178452749, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl Benzoate | HCID 7150 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | tert-Butyl (4-acetylphenyl)carbamate | HCID 15373979 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178452749 | HCID 178452749 | 83.5% |
Reaction Steps
NaH (60% dispersion, 0.388 g, 16.2 mmol) was added to a solution of methyl benzoate (0.629 g, 4.62 mmol) and 1,1-dimethylethyl (4-acetylphenyl)carbamate (N-BOC-4-aminoacetophenone 1.09 g, 4.62 mmol) in anhydrous DMF (20 mL) at 0° C. The reaction was allowed to warm to room temperature overnight then quenched with saturated aqueous NH4Cl and neutralized with 1M HCl. The reaction was diluted with ethyl acetate (80 mL) and the organic layer washed successively with saturated aqueous NaHCO3 and brine. The organic phase was separated and dried over Na2SO4, filtered, and concentrated in vacuo to provide the condensation product as a yellow oil (1.31 g, 83% yield). The product was used in the subsequent step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08710038B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-a1e706f2a72d4e50ac972fff794bf634 |
| Source note | uspto-grants-2014_04 |