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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 848409Generated: October 29, 2026

Iodoethane → 3-Ethylhexahydro-3-(3-methoxyphenyl)-1-methyl-2H-azepin-2-one

https://huagongshe.com/reaction/848409

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
Reactant2-ChloroanisoleHCID 13011—
Reactant2,2,6,6-TetramethylpiperidineHCID 13035—
ReactantN-MethylcaprolactamHCID 17369—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product3-Ethylhexahydro-3-(3-methoxyphenyl)-1-methyl-2H-azepin-2-oneHCID 2729097—

Reaction Steps

a solution of butyl lithium (0.05 mole) in hexane (31.25 ml) was treated with 2,2,6,6-tetramethylpiperidine (8.5 ml), followed by dry tetrahydrofuran ("THF"; 100 ml) under an inert atmosphere at 0° C. The mixture was treated with a solution of N-methylcaprolactam (6.25 ml, 50 mM) in THF (20 ml) and stirred for 30 minutes. A solution of butyl lithium (0.05 mole) in hexane (31.25 ml), was added and the mixture stirred for 15 minutes. A solution of o-chloroanisole (6.2 ml) in THF (20 ml) was added slowly, the mixture stirred for 1.5 hours and treated with ethyl iodide (5.15 ml). After one hour, the reaction was quenched with water (100 ml) and the solvents removed under reduced pressure. The residue was partitioned between 2 N HCl (200 ml) and toluene (250 ml). The organic layer was washed with brine, dried and the solvents removed under reduced pressure, to give 3-ethylhexahydro-3-(3 -methoxyphenyl)-1-methyl-2H-azepin-2-one (5.5 g) b.p. 140°/0.1 mm. Recrystallisation from diisopropyl ether gave pure title compound (5.0 g) m.p. 68°-69° C., identical with authentic material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04296029
Source datasetuspto-grants-1981_10
ORD IDord-3c721d953e264fa383fefad10a01c453
Source noteuspto-grants-1981_10