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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5391Generated: October 27, 2026

Iodine → cis Ethyl 3-bromo-2-oxo-1-azacyclodecane-10-carboxylate

https://huagongshe.com/reaction/5391

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantBromineHCID 24408—
ReactantPhosphorus pentachlorideHCID 24819—
ReactantEthyl 2-oxo-1-azacyclodecane-10-carboxylateHCID 19930826—
SolventDichloromethaneHCID 6344—
Productcis Ethyl 3-bromo-2-oxo-1-azacyclodecane-10-carboxylateHCID 131718120—

Reaction Conditions

Temperature0 °C

Reaction Steps

Ethyl 2-oxo-1-azacyclodecane-10-carboxylate (4.0 g, 17.6 mmol) is dissolved in methylene chloride (50 mL), and cooled to 0° C. Phosphorus pentachloride (3.85 g, 18.5 mmol) and iodine (0.051 g, 0.2 mmol) are added. The reaction is stirred for 15 minutes at 0° C. Then, bromine (3.10 g, 19.4 mmol) is added, and the reaction is stirred at 0° C. for 4 hours. The reaction is quenched by adding saturated sodium sulfite (until the color of excess bromine disappears), and extracted several times with methylene chloride. The combined organic layers are dried (Na2SO4), and the solvent is evaporated. The product is purified by silica gel chromatography (15% ethyl acetate/hexane) to give cis ethyl 3-bromo-2-oxo-1-azacyclodecane-10-carboxylate, m.p. 132°-134° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05244889
Source datasetuspto-grants-1993_09
ORD IDord-506b9adb631a461cb9ffccba8d2f7bb0
Source noteuspto-grants-1993_09