HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetoacetate → Ethyl 3-oxo-5-m-toluylpentanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetoacetate | HCID 8868 | — |
| Reactant | m-Xylyl bromide | HCID 12099 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 3-oxo-5-m-toluylpentanoate | HCID 54309110 | — |
Reaction Steps
Ethyl acetoacetate (74.5 ml) was added dropwise to a solution of lithium diisopropylamide (2.0M solution in heptane/tetrahydrofuran/ethylbenzene, 600 ml) in tetrahydrofuran (2.5 L) at 0° C. The mixture was stirred for 30 min then 3-methylbenzylbromide (79 ml) was added dropwise. The mixture was stirred for 1 hour at 0° C. then quenched with 2M HCl. The mixture was extracted with ethyl acetate, the extracts washed with water, dried (MgSO4) and evaporated to give an oil which was purified by chromatography eluting with 5-10% ethyl acetate in isohexane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06218376B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-4567031854d64034950188e2e4720135 |
| Source note | uspto-grants-2001_04 |