HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → Ethyl 4-(2,4-dichlorophenyl)-2,4-dioxobutanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 2',4'-Dichloroacetophenone | HCID 16693 | — |
| Reactant | Acetoxyacetyl chloride | HCID 26297 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Product | Ethyl 4-(2,4-dichlorophenyl)-2,4-dioxobutanoate | HCID 22997478 | — |
Reaction Conditions
| Temperature | -78 °C |
|---|
Reaction Steps
A solution of 2,4-dichloroacetophenone (3.78 g) in THF (20 ml) was cooled to −78° C. under a nitrogen atmosphere. To this stirred solution was added lithium diisopropylamide (LDA) (1.0 M, 22 ml) and the resulting solution was stirred at −78° C. for 15 minutes. Acetoxyacetyl chloride (2.3 ml) was injected and the mixture was stirred for 1 hour and then allowed to warm to room temperature. The reaction was quenched with 1N HCl and the product was extracted with diethyl ether (200 ml). The organic layer was dried, concentrated and recrystallized from ether/hexanes, yielding ethyl 4-(2,4-dichlorophenyl)-2,4-diketobutyrate (intermediate 1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06613777B1 |
| Source dataset | uspto-grants-2003_09 |
| ORD ID | ord-c18014cf62e6472a80820d149fbcfe83 |
| Source note | uspto-grants-2003_09 |