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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | 2-Chloroanisole | HCID 13011 | — |
| Reactant | 2,2,6,6-Tetramethylpiperidine | HCID 13035 | — |
| Reactant | 1-Trimethylsilanyl-azepan-2-one | HCID 11423999 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Ethyl-3-(3-methoxyphenyl)azepan-2-one | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06316436B1 |
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| Source dataset | uspto-grants-2001_11 |
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| ORD ID | ord-382a25474c234a80afc519e85113c9d9 |
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| Source note | uspto-grants-2001_11 |
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