化工社化工社 化学情報印刷レポート · 研究参考用
Acetic Anhydride → 3(-1-Acetoxytridecyl)-4-phenylfuran
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Acetic Anhydride | HCID 7918 | — |
| 反応物 | 4-Phenyl-3-furaldehyde | HCID 15037148 | — |
| 反応物 | HCID 178443215 | HCID 178443215 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 3(-1-Acetoxytridecyl)-4-phenylfuran | HCID 15037156 | — |
反応手順
Dodecylmagnesium bromide (a 1.0M solution in THF; 2.11 ml, 2.11 mmol) was added to a solution of 4-phenyl-3-furaldehyde (303 mg, 1.76 mmol) in THF at 0 degrees under argon and gradually allowed to warm to room temperature with stirring. When all of the aldehyde was consumed acetic anhydride (719 mg, 7.04 mmol) was added and stirring was continued for 2 hours more. The reaction was quenched with saturated ammonium chloride and the organics were extracted into ethyl ether. The combined fractions were washed with saturated sodium bicarbonate, water and brine, dried over magnesium sulfate and concentrated to a yellow oil which was purified by flash chromatography on silica using 3% ethyl ether hexanes to give the title compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05268387 |
| 出典データセット | uspto-grants-1993_12 |
| ORD ID | ord-3eef5af2d972410ea16ff6997ef0445c |
| 出典メモ | uspto-grants-1993_12 |