HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl Acrylate → methyl (RS)-5-(3-iodophenyl)-4-(2-methylphenyl)-5-oxopentanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl Acrylate | HCID 7294 | — |
| Reactant | 1-(3-Iodophenyl)-2-(2-methylphenyl)ethanone | HCID 22010198 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | methyl (RS)-5-(3-iodophenyl)-4-(2-methylphenyl)-5-oxopentanoate | HCID 54018710 | — |
Reaction Steps
A solution of 1-(3-iodophenyl)-2-(2-methylphenyl)ethanone (3.21 g) in dry tetrahydrofuran (30 mL) is treated with methyl acrylate (0.9 mL) and potassium tertiary butoxide (0.107 g). The reaction mixture is heated at reflux for 18 hours, evaporated and the residue partitioned between ethyl acetate (60 mL) and water (30 mL). The organic phase is dried over magnesium sulphate, evaporated and the residual solid washed with pentane to give methyl (RS)-5-(3-iodophenyl)-4-(2-methylphenyl)-5-oxopentanoate as a fawn coloured solid (3.39 g), m.p. 106-108° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06211234B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-671d0db8208e4f7f86bcf4d3aca56add |
| Source note | uspto-grants-2001_04 |