化工社化工社 化学情報印刷レポート · 研究参考用
p-Toluenesulfonic acid monohydrate → 5-isocyano-2,3-dihydroinden-1-one O-tert-butyldimethylsilyl oxime
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| 反応物 | O-(tert-Butyldimethylsilyl)hydroxylamine | HCID 4691350 | — |
| 反応物 | 5-Isocyano-2,3-dihydroinden-1-one | HCID 18719813 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 生成物 | 5-isocyano-2,3-dihydroinden-1-one O-tert-butyldimethylsilyl oxime | HCID 57762062 | 75% |
反応手順
5-isocyano-2,3-dihydroinden-1-one (6) (3.00 g, 19.1 mmol) was combined with 1.4 eq. of O-(tert-butyldimethylsilyl)hydroxylamine (3.94 g, 26.7 mmol) and TsOH-H2O (0.363 g, 1.91 mmol) in 100 mL CHCl3 and heated to reflux overnight. TLC showed a small amount of remaining starting material and two non-polar spots corresponding to the oxime isomers. The reaction mixture was filtered and concentrated to a brown semi-solid, then purified immediately by loading onto a silica column with DCM and eluting with 1% MeOH/DCM to give 4.1 g (75%) of 5-isocyano-2,3-dihydroinden-1-one O-tert-butyldimethylsilyl oxime (7).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07566716B2 |
| 出典データセット | uspto-grants-2009_07 |
| ORD ID | ord-ae9251e2d047444d975d8e416a707f52 |
| 出典メモ | uspto-grants-2009_07 |