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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 74994Erstellt: 25. Oktober 2026

Iodine → 4-Iodo-1-methyl-6-azabicyclo[3.2.1]octan-7-one

https://huagongshe.com/reaction/74994

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
EduktTriethylamineHCID 8471—
EduktTrimethylsilyl triflateHCID 65367—
Edukt1-Methylcyclohex-3-ene-1-carboximidic acidHCID 3052840—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelPentaneHCID 8003—
Produkt4-Iodo-1-methyl-6-azabicyclo[3.2.1]octan-7-oneHCID 67286126—

Reaktionsschritte

A solution of 1-methylcyclohex-3-ene-1-carboxamide, 52b, (5.0 g, 35.9 mmol) dissolved in 100 mL of pentane and CH2Cl2 was cooled to 0° C. and treated with triethylamine (11.0 mL, 79.0 mmol) and trimethylsilyl-triflate (14.3 mL, 79.0 mmol) sequentially. The resulting mixture was stirred for 1 hour at room temperature. The lower layer was removed via pipette. The upper pentane layer was concentrated in vacuo and the resulting residue was dissolved in THF (100 mL). To the stirred reaction was added iodine (20.1 g, 79.02 mmol) and the reaction was allowed to stir overnight at room temperature. After quenching with Na2SO3 and NaHCO3, the reaction was partitioned between CH2Cl2 and water. The organic layers were combined, dried over Na2SO4, concentrated in vacuo to a dark yellow oil (9.5 g) that was used without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08829007B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-77fac139931c443595455cd9f7021773
Quellennotizuspto-grants-2014_09