化工社化工社 化学情報印刷レポート · 研究参考用
Dimethylformamide → 2,2-Dimethylbenzo[d][1,3]dioxole-5-carbaldehyde
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | Hexane | HCID 8058 | — |
| 反応物 | 4-Cyclopropylbenzaldehyde | HCID 11506474 | — |
| 反応物 | 5-Bromo-2,2-dimethylbenzo(d)(1,3)dioxole | HCID 11593803 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 生成物 | 2,2-Dimethylbenzo[d][1,3]dioxole-5-carbaldehyde | HCID 596012 | 83% |
反応手順
The title compound was synthesized in analogy to 4-cyclopropyl benzaldehyde (described in example S53) using 420 mg of 5-bromo-2,2-dimethyl-benzo[1,3]dioxole [CAS 73790-19-9] (1.83 mmol), 1.38 ml of a 1.6 molar solution of n-BuLi in hexane (2.20 mmol) and 712 μl of DMF (9.17 mmol). The isolated residue was purified by flash column chromatography (1:9 ether/pentane) to give 270 mg of 2,2-dimethyl-benzo[1,3]dioxole-5-carbaldehyde (83%) as a light yellow liquid. 1H NMR (CDCl3, 300 MHz): δ 1.72 (s, 6H), 6.84 (d, J=7.8 Hz, 1H), 7.26 (s, 1H), 7.87 (dd, J=8.0 and 1.7 Hz, 1H), 9.97 (s, 1H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07259183B2 |
| 出典データセット | uspto-grants-2007_08 |
| ORD ID | ord-133379b692704aecb11964eb767736a5 |
| 出典メモ | uspto-grants-2007_08 |