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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21965Generated: October 25, 2026

Ethyl 2,3-di-oxo-1-azacyclodecane-10-carboxylate → Ethyl 3-(trimethylsilylmethyl)-3-hydroxy-2-oxo-1-azacyclodecane-10-carboxylate

https://huagongshe.com/reaction/21965

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2,3-di-oxo-1-azacyclodecane-10-carboxylateHCID 19930804—
ReactantHCID 178418680HCID 178418680—
SolventDiethyl EtherHCID 3283—
ProductEthyl 3-(trimethylsilylmethyl)-3-hydroxy-2-oxo-1-azacyclodecane-10-carboxylateHCID 19930812—

Reaction Conditions

Temperature0 °C

Reaction Steps

Ethyl 2,3-di-oxo-1-azacyclodecane-10-carboxylate (5.02 g, 20.81 mmol) is dissolved in ether (50 mL), and cooled to 0° C. Trimethylsilylmethylmagnesium chloride (42.0 mL of a 1.0M solution in ether, 42.0 mmol) is added dropwise, the reaction is stirred at 0° C. for 20 minutes, and then heated to reflux overnight. The reaction is quenched with saturated ammonium chloride, and extracted several times with ethyl acetate. The combined organic layers are dried (Na2SO4), and the solvent is evaporated. The product is purified by silica gel chromatography (10% ethyl acetate/hexane) to give separately the two diastereomers of ethyl 3-(trimethylsilylmethyl)-3-hydroxy-2-oxo-1-azacyclodecane-10-carboxylate; major isomer, m.p. 129°-130° C.; minor isomer, m.p. 175°-177° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05426103
Source datasetuspto-grants-1995_06
ORD IDord-a31e8b575c884584a0ca2bedb89b6bf4
Source noteuspto-grants-1995_06