関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Iodine | HCID 807 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Trimethylsilyl triflate | HCID 65367 | — |
| 反応物 | 1-Methylcyclohex-3-ene-1-carboximidic acid | HCID 3052840 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 溶媒 | Pentane | HCID 8003 | — |
| 生成物 | 4-Iodo-1-methyl-6-azabicyclo[3.2.1]octan-7-one | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US09345708B2 |
|---|
| 出典データセット | uspto-grants-2016_05 |
|---|
| ORD ID | ord-4e533b5a68504ea2938d3df58ddee90b |
|---|
| 出典メモ | uspto-grants-2016_05 |
|---|