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Indole → 6-(1H-indol-3-yl)hexanoic acid
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Indole | HCID 798 | — |
| 反応物 | Water | HCID 962 | — |
| 反応物 | epsilon-CAPROLACTONE | HCID 10401 | — |
| 反応物 | Potassium Hydroxide | HCID 14797 | — |
| 溶媒 | P-Cymene | HCID 7463 | — |
| 生成物 | 6-(1H-indol-3-yl)hexanoic acid | HCID 4672789 | — |
反応手順
In a water separator, indole (50 g, 0.43 mol.), ε-caprolactone (oxepan-2-one, 55.9 g, 0.49 mol.), potassium hydroxide (35.9 g, 0.64 mol.) in p-cymene (1-isopropyl-4-methylbenzene, 250 ml) were heated at boiling for 4 d, with stirring. For working up, water (200 ml) was added to the mixture, the phases were separated, and the aqueous phase was adjusted to pH 4 with 2M HCl and stored for 2 d at 4° C. in a refrigerator. The resulting solid was filtered off with suction and washed with water (3×20 ml). Recrystallisation from ether (50 ml) yielded 6-(1H-indol-3-yl)hexanoic acid in the form of a white solid having a melting point of 124–126° C. in a yield of 16.9 g.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07173045B2 |
| 出典データセット | uspto-grants-2007_02 |
| ORD ID | ord-ada1d4d81014435da937c72e3ca1084d |
| 出典メモ | uspto-grants-2007_02 |