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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1594856Generated: October 31, 2026

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

https://huagongshe.com/reaction/1594856

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 Example 5, Step A) (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 numberUS06284755B1
Source datasetuspto-grants-2001_09
ORD IDord-b8cd4b2059014282831a97a37fa73b67
Source noteuspto-grants-2001_09