HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 1-Trichloromethyl-3-methyl-2-butenyl 2-diazoacetoacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Trichloromethyl-3-methyl-2-butenyl acetoacetate | HCID 12525203 | — |
| Reactant | Sulfuryl diazide | HCID 15191028 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-Trichloromethyl-3-methyl-2-butenyl 2-diazoacetoacetate | HCID 54462030 | 96% |
Reaction Steps
To a solution of 1-trichloromethyl-3-methyl-2-butenyl acetoacetate (0.575 g, 2 mmole) and triethylamine (0.404 g, 4 mmole) in 10 ml of acetonitrile was added 1 g of polymer-bound sulfonyl azide (prepared by the method of Roush, et al., loc. cit.). The mixture was stirred overnight at room temperature and filtered. The filter cake was washed with ether, and the slurry was filtered. Solvent was removed by evaporation from the combined filtrates to give 1-trichloromethyl-3-methyl-2-butenyl 2-diazoacetoacetate (0.60 g, 96% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04526987 |
| Source dataset | uspto-grants-1985_07 |
| ORD ID | ord-5d2c72f3fff8409dbd9c1050b719bf40 |
| Source note | uspto-grants-1985_07 |