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Diiodomethane → 2-Iodo-1,3-dinitrobenzene
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Diiodomethane | HCID 6346 | — |
| 反応物 | 2,6-Dinitroaniline | HCID 69070 | — |
| 生成物 | 2-Iodo-1,3-dinitrobenzene | HCID 14571184 | 52% |
反応手順
To a dispersion of 2,6-dinitroaniline (4.00 g, 0.021 mol) in diiodomethane (24 mL, 0.297 mol) isoamylnitrite (15 mL, 0.112 mol) was added (Smith et al., 1990, which is incorporated herein by reference). The mixture was stirred at room temperature for one hour, and then heated at 105° C. for eight hours. The excess of diiodomethane was removed in high vacuo. The residue was diluted with acetyl acetate (10 mL). Silica (ca 30 mL, mesh 230-400 Å) was added; the mixture was concentrated in vacuo and purified by column chromatography to yield 1-iodo-2,6-dinitrobenzene (3.21 g, 52%). 1H NMR (400 MHz, CDCl3): δ 7.84 (d, 2 H, J=8.0 Hz), 7.67 (t, 1 H, J=8.0 Hz).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08497360B2 |
| 出典データセット | uspto-grants-2013_07 |
| ORD ID | ord-10d042ef3af74fec831be2a65394c4db |
| 出典メモ | uspto-grants-2013_07 |