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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5390Generated: October 25, 2026

Methanesulfonic Acid → Ethyl 2-oxo-1-azacyclodecane-10-carboxylate

https://huagongshe.com/reaction/5390

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
ReactantAmmonium HydroxideHCID 14923—
ReactantSodium AzideHCID 33557—
ReactantEthyl 2-oxocyclononanecarboxylateHCID 107210—
SolventChloroformHCID 6212—
ProductEthyl 2-oxo-1-azacyclodecane-10-carboxylateHCID 19930826—

Reaction Conditions

Temperature0 °C

Reaction Steps

2-Ethoxycarbonyl-cyclononanone (13.72 g, 64.7 mmol) is dissolved in chloroform (200 mL) and cooled to 0° C. Methanesulfonic acid (62.4 g, 650 mmol) is added, followed by sodium azide (12.68 g, 195 mmol). The reaction is stirred at room temperature for 30 minutes, and then heated to reflux for 4 hours. The reaction mixture is poured onto ice, made basic with concentrated ammonium hydroxide (pH=9), and extracted several times with methylene chloride. The combined organic layers are dried (MgSO4), and the solvent is evaporated. The product is purified by silica gel chromatography (40% ethyl acetate/hexane) to give ethyl 2-oxo-1-azacyclodecane-10-carboxylate, m.p. 101°-103° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05244889
Source datasetuspto-grants-1993_09
ORD IDord-457a83af2b8e486aa8de7028583f3486
Source noteuspto-grants-1993_09