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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 555674Generated: October 26, 2026

Iodoethane → Ethyl 4-(benzyloxycarbonylamino)bicyclo[2.2.2]octane-1-carboxylate

https://huagongshe.com/reaction/555674

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantSodium BicarbonateHCID 516892—
Reactant4-(Benzyloxycarbonylamino)bicyclo[2.2.2]octane-1-carboxylic acidHCID 10662201—
SolventDimethylformamideHCID 6228—
ProductEthyl 4-(benzyloxycarbonylamino)bicyclo[2.2.2]octane-1-carboxylateHCID 10616503—

Reaction Conditions

Temperature55 °C

Reaction Steps

4-Benzyloxycarbonylaminobicyclo[2.2.2]octane-1-carboxylic acid (56.0 g) was dissolved in N,N-dimethylformamide (1000 mL). To this solution, sodium bicarbonate (46.6 g) and then ethyl iodide (22.2 mL) were added and the mixture was stirred at 50 to 60° C. for 5 hours. Subsequently, additional sodium bicarbonate (46.6 g) and ethyl iodide (22.2 mL) were added and the mixture was stirred for additional 3 hours. The insoluble materials in the mixture were filtered and the filtrate was concentrated under reduced pressure. The residue was dissolved in ethyl acetate (700 mL) and the solution was washed with water, dried over anhydrous sodium sulfate, and dried under reduced pressure. The resulting residue was purified by silica gel column chromatography (eluant:hexane:ethyl acetate=2:1→ethyl acetate) to give ethyl 4-benzyloxycarbonylamino-bicyclo[2.2.2]octane-1-carboxylate (56.8 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08053465B2
Source datasetuspto-grants-2011_11
ORD IDord-a38c88ba70774c17966c50e895a4d7ac
Source noteuspto-grants-2011_11