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HRID 527022作成日:2026年10月25日

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

https://huagongshe.com/reaction/527022

反応式

関与物質

役割名称HCID仕込み量
反応物IodineHCID 807—
反応物TriethylamineHCID 8471—
反応物Trimethylsilyl triflateHCID 65367—
反応物1-Methylcyclohex-3-ene-1-carboximidic acidHCID 3052840—
溶媒DichloromethaneHCID 6344—
溶媒PentaneHCID 8003—
生成物4-Iodo-1-methyl-6-azabicyclo[3.2.1]octan-7-oneHCID 67286126—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09345708B2
出典データセットuspto-grants-2016_05
ORD IDord-4e533b5a68504ea2938d3df58ddee90b
出典メモuspto-grants-2016_05