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 | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 54155424 | HCID 54155424 | 37.4% |
Reaction Steps
To a solution of 43.79 g acetic acid 3-(4-tert-butyl-phenyl)-2-methyl-propenyl ester in 200 ml of tetrahydrofuran, a solution of 27.16 g potassium tert-butoxide in 200 ml of tetrahydrofuran was added at −78° C. After stirring at this temperature for 90 minutes, a solution of 53.00 g 4-oxo-undecanoyl chloride in 200 ml of tetrahydrofuran was added. After stirring at −78° C. for 2.5 hours, the solution was quenched with saturated sodium bicarbonate solution and diluted with ether. The organic phase was washed with saturated sodium bicarbonate solution and brine, dried and evaporated to dryness. The residue was purified by thin-film distillation and chromatography to yield 25.73 g of a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06479682B1 |
| Source dataset | uspto-grants-2002_11 |
| ORD ID | ord-d8bd35504fa242419eac4313dd5bf1f6 |
| Source note | uspto-grants-2002_11 |