化工社化工社 化学情報印刷レポート · 研究参考用
1,4-Dioxane → Ketone, 3-furyl phenyl
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1,4-Dioxane | HCID 31275 | — |
| 反応物 | 3-Bromobenzaldehyde | HCID 76583 | — |
| 反応物 | Potassium Fluoride | HCID 522689 | — |
| 反応物 | 2-(Tributylstannyl)furan | HCID 4393688 | — |
| 触媒 | HCID 178418476 | HCID 178418476 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | Ketone, 3-furyl phenyl | HCID 201640 | 86% |
反応手順
EX-592A) To a dioxane (20 mL) solution of 3-bromobenzaldehyde (0.63 mL, 5.4 mmol) was added 2-(tributylstannyl)furan (1.89 ml, 6.00 mL) and Pd(PPh3)2Cl2 (0.21 g, 0.30 mmol). The mixture was heated to reflux under argon for 1.5 h. The cooled mixture was poured into a mixture of saturated KF and ethyl acetate and stirred 18 h. The slurry was filtered through celite. The organic layer was separated, washed with brine, dried (MgSO4) and evaporated to an oil. Purification by flash chromatography on silica gel eluting with 5% ethyl acetate in hexane gave 0.80 g (86%) of the desired 3-(2-furanyl)benzaldehyde product as an yellow oil which solidified upon standing. MS: m/z=173.1 [M+H]+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06458803B1 |
| 出典データセット | uspto-grants-2002_10 |
| ORD ID | ord-b2b3f0360fd34d9594dfe1154a35c509 |
| 出典メモ | uspto-grants-2002_10 |