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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21962Generated: October 26, 2026

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

https://huagongshe.com/reaction/21962

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 numberUS05426103
Source datasetuspto-grants-1995_06
ORD IDord-0576b060cf1e471fa22125ca94b64b1f
Source noteuspto-grants-1995_06