HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl diazoacetate → Ethyl 2-tert-butoxy-3-(5-methylpyridin-2-yl)cyclopropanecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl diazoacetate | HCID 12192 | — |
| Reactant | (Z)-2-(2-tert-butoxyvinyl)-5-methylpyridine | HCID 86729575 | — |
| Catalyst | Copper Sulfate | HCID 24462 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Ethyl 2-tert-butoxy-3-(5-methylpyridin-2-yl)cyclopropanecarboxylate | HCID 71271320 | 34% |
Reaction Steps
The solution of (Z)-2-(2-tert-butoxyvinyl)-5-methylpyridine (12-3) (1.20 g, 6.27 mmol) in toluene (20 mL) and anhydrous copper sulfate (100 mg, 0.63 mmol) was heated to 75° C. Then the solution of ethyl diazoacetate (2.17 g, 18.8 mmol) in toluene (10 mL) was added dropwise over 2 h. It was heated for another 2 h after the addition was completed. The mixture was restored to room temperature for overnight. The solvent was removed under reduced pressure and the residue was purified by silca gel chromatography with gradient eluent (PE/EA=40/1; 20/1; 10/1). The product was obtained as a yellow oil (500 mg, 34%). LRMS (ES) calculated M+H for C16H24NO3: 278.3. Found: 278.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09062059B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-99e517fbd9d048e5ab1d10103465dc69 |
| Source note | uspto-grants-2015_06 |