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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Phosphorus pentachloride | HCID 24819 | — |
| Reactant | Ethyl 2-oxo-1-azacyclodecane-10-carboxylate | HCID 19930826 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | cis Ethyl 3-bromo-2-oxo-1-azacyclodecane-10-carboxylate | HCID 131718120 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05426103 |
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| Source dataset | uspto-grants-1995_06 |
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| ORD ID | ord-ae6e3feffc3748f18ceeb2c6741450df |
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| Source note | uspto-grants-1995_06 |
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