HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dodecanoyl chloride → HCID 86592258, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dodecanoyl chloride | HCID 8166 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Chloro-7-hydroxy-4-methyl-2-benzopyrone | HCID 5355079 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86592258 | HCID 86592258 | — |
Reaction Steps
2.5 g of 3-chloro-4-methyl-7-hydroxy coumarin was dissolved in 60 ml of tetrahydrofuran in a 250 ml flask, followed by the addition of 3.6 g of potassium carbonate and 3.6 ml of triethylamine. After 30 minutes, 8.0 ml of lauroyl chloride was added thereto and the mixture was stirred for 2 hours at room temperature. Thereafter, 50 ml of distilled water and 250 ml of ethyl acetate were added to extract the title compound into the ethyl acetate phase. The ethyl acetate phase was washed with 200 ml of salt water, and then dried with anhydrous manganese. Following the distillation and evaporation of the solvent, the residue was recrystalized with hexane and ethyl acetate to obtain white 3-chloro-4-methyl-7-hydroxy coumarin laurate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06991914B2 |
| Source dataset | uspto-grants-2006_01 |
| ORD ID | ord-a109dfee3478408387f7f6789f328bc1 |
| Source note | uspto-grants-2006_01 |