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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 429067Generated: October 30, 2026

Iodoethane → 3-Ethyl-3-(3-methoxyphenyl)azepan-2-one

https://huagongshe.com/reaction/429067

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantHexaneHCID 8058—
Reactant2-ChloroanisoleHCID 13011—
Reactant2,2,6,6-TetramethylpiperidineHCID 13035—
Reactant1-Trimethylsilanyl-azepan-2-oneHCID 11423999—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product3-Ethyl-3-(3-methoxyphenyl)azepan-2-oneHCID 2815455—

Reaction Steps

To 1.6 M n-BuLi in hexane (31.3 mL, 50 mmol) at 0° C. was added a solution of 2,2,6,6-tetramethyl piperidine (8.43 mL, 50 mmol) in anhydrous THF (100 mL) over 5 min. 1-Trimethylsilanyl-azepan-2-one (as described in Step F above) (9.26 g, 50 mmol) in anhydrous THF (20 mL) was added. After stirring the reaction mixture for 10 min, a further portion of 1.6M n-BuLi in hexane (31.3 mL, 50 mmol) was added, the mixture stirred for 10 min, and 2-chloroanisole (6.34 mL, 50 mmol) was added. After stirring for 30 min under Ar, ethyl iodide (3.90 mL, 48.7 mmol) was added, the reaction mixture was stirred for 30 min, quenched with H2O, concentrated in vacuo, diluted with EtOAc, and washed with 5N HCl (100 mL) and brine. The organic layer was dried (MgSO4), concentrated and purified using SiO2 chromatography (10-15% EtOAc/CH2Cl2) to give the title compound

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06316436B1
Source datasetuspto-grants-2001_11
ORD IDord-382a25474c234a80afc519e85113c9d9
Source noteuspto-grants-2001_11