Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21963Generated: October 25, 2026

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

https://huagongshe.com/reaction/21963

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 numberUS05426103
Source datasetuspto-grants-1995_06
ORD IDord-ae6e3feffc3748f18ceeb2c6741450df
Source noteuspto-grants-1995_06