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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339038Generated: October 26, 2026

Chlorotrimethylsilane → Ethyl 3-methyl-3-(2-methylquinolin-8-yl)butanoate

https://huagongshe.com/reaction/339038

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
Reactant(Z)-ethyl 3-(2-methylquinolin-8-yl)but-2-enoateHCID 70983529—
ReactantHCID 178418348HCID 178418348—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
ProductEthyl 3-methyl-3-(2-methylquinolin-8-yl)butanoateHCID 7098454876.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a mixture of Cu(I)I (2.42 g, 12.7 mmol) in ether (5 mL) was added a solution of 1.6 M MeLi (15.9 ml, 25.4 mmol) in ether at 0° C. and the mixture was stirred at 0° C. for 10 minutes. The solvent was removed under reduced pressure and cold DCM (10 mL) was added. The solvent was removed under reduced pressure. Cold DCM (40 mL) was added and the mixture was cooled to −78° C. TMSCl (1.54 mL, 12.7 mmol) was added, followed by a solution of (Z)-ethyl 3-(2-methylquinolin-8-yl)but-2-enoate (0.81 g, 3.17 mmol) in DCM (10 mL). The reaction mixture was warmed to 0° C. and stirred at 0° C. for 1 hour. The reaction mixture was quenched with saturated ammonium chloride solution. The organic layers was separated, washed with brine, dried (sodium sulfate), filtered and concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel (7:1 hexane/ethyl acetate) to give ethyl 3-methyl-3-(2-methylquinolin-8-yl)butanoate (0.66 g, 76.8%) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889704B2
Source datasetuspto-grants-2014_11
ORD IDord-55b88b37eeb64b3bbff75d0f0ece3621
Source noteuspto-grants-2014_11