HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1515195Erstellt: 27. Oktober 2026
Iodine → (2-Aminophenyl)(1-methylpiperidin-4-yl)methanone
https://huagongshe.com/reaction/1515195
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Iodine | HCID 807 | — |
| Edukt | Tetrahydrofuran | HCID 8028 | — |
| Edukt | 2-Aminobenzonitrile | HCID 72913 | — |
| Edukt | 4-chloro-N-methylpiperidine | HCID 79342 | — |
| Edukt | Magnesium | HCID 5462224 | — |
| Edukt | HCID 178478990 | HCID 178478990 | — |
| Produkt | (2-Aminophenyl)(1-methylpiperidin-4-yl)methanone | HCID 21414385 | 7% |
Reaktionsschritte
To a suspension of magnesium (1.8 g, 74 mmol) in dry THF (50 mL) in a flame-dried round bottomed flask under nitrogen was added 4-chloro-1-methylpiperidine (9.0 g, 68 mmol). A crystal of iodine and a catalytic amount of cyclohexylmagnesium chloride was added and the mixture was heated to reflux for 2 h. A gray precipitate formed, which was removed via vacuum filtration under a nitrogen atmosphere. To the filtrate was added a solution of 2-aminobenzonitrile (1.6 g, 14 mmol) in dry THF (15 mL). The stirred mixture was heated to 45° C. for 2 h. Ice was added and the reaction was quenched with 1 M sulfuric acid. The mixture was extracted with ethyl acetate and the acidic aqueous layer was then neutralized with 1 N sodium hydroxide, concentrated on a rotary evaporator and extracted with ethyl acetate. The combined organics were dried over sodium sulfate, filtered and concentrated to afford (2-aminophenyl)(1-methylpiperidin-4-yl)methanone as a yellow oil (1.0 g, 7%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08222263B2 |
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| Quelldatensatz | uspto-grants-2012_07 |
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| ORD ID | ord-12e0fd4664a249cfbff59d2a38280fbb |
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| Quellennotiz | uspto-grants-2012_07 |
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