HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Oxo-undecanoyl Chloride → HCID 54155424, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Oxo-undecanoyl Chloride | HCID 22990500 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | Acetic Acid 3-(4-tert-butyl-phenyl)-2-methyl-propenyl Ester | HCID 53757095 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 54155424 | HCID 54155424 | 37.4% |
Reaction Steps
A solution of 43.79 g acetic acid 3-(4-tert-butyl-phenyl)-2-methyl-propenyl ester in 200 ml of THF was cooled to −70° C. A solution of 27.16 g potassium-tert-butoxide in 200 ml of THF was added at −70° C. during 20 min. and the resulting reaction mixture was stirred for 90 min. at the same temperature. Then a solution of 53.00 g 4-oxo-undecanoyl chloride in 200 ml of THF was dropped in and the reaction mixture was stirred for another 2.5 hours at −70° C. Then the reaction mixture was diluted with ether, washed with saturated NaHCO3 and brine. The organic phase was dried, filtered and evaporated to dryness. The residue was thin-layer distilled and purified by chromatography to yield 25.73 g of a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06207857B1 |
| Source dataset | uspto-grants-2001_03 |
| ORD ID | ord-aa1572beb9224bd982ab75748bd6b4b4 |
| Source note | uspto-grants-2001_03 |