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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl 2,3-di-oxo-1-azacyclodecane-10-carboxylate | HCID 19930804 | — |
| Reactant | HCID 178418680 | HCID 178418680 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Ethyl 3-(trimethylsilylmethyl)-3-hydroxy-2-oxo-1-azacyclodecane-10-carboxylate | HCID 19930812 | — |
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
| 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-a31e8b575c884584a0ca2bedb89b6bf4 |
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| Source note | uspto-grants-1995_06 |
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