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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175421Generated: October 30, 2026

Ethyl diazoacetate → Ethyl 2-tert-butoxy-3-(5-methylpyridin-2-yl)cyclopropanecarboxylate

https://huagongshe.com/reaction/2175421

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl diazoacetateHCID 12192—
Reactant(Z)-2-(2-tert-butoxyvinyl)-5-methylpyridineHCID 86729575—
CatalystCopper SulfateHCID 24462—
SolventTolueneHCID 1140—
ProductEthyl 2-tert-butoxy-3-(5-methylpyridin-2-yl)cyclopropanecarboxylateHCID 7127132034%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062059B2
Source datasetuspto-grants-2015_06
ORD IDord-99e517fbd9d048e5ab1d10103465dc69
Source noteuspto-grants-2015_06