Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Delta-Valerolactone | HCID 10953 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 5-Fluoroindole | HCID 67861 | — |
| Solvent | P-Cymene | HCID 7463 | — |
| Product | HCID 21082138 | HCID 21082138 | 21.8% |
Reaction Steps
In a water separator, 5-fluoroindole (5.0 g, 37 mmol.), δ-valerolactone (3.83 ml, 42 mmol.), potassium hydroxide (3.09 g, 55 mmol.) in p-cymene (120 ml) were heated to boiling, with stirring. The water separation was stopped after 80 h. For working up, water (50 ml) was added to the mixture at RT and stirring was carried out for 30 min. The phases were then separated in a separating funnel. The aqueous phase was washed with ether (3×20 ml), adjusted to pH 1 with 2M HCl and extracted with ether (5×25 ml). The combined extracts were washed with water (5×10 ml), dried, filtered and concentrated. The residue was purified by flash chromatography on silica gel (375 g) (eluant: 2700 ml of cyclohexane/EE 4:1 followed by 1500 ml of cyclohexane/EE 1:1 and 650 ml of EE). 1.9 g of 5-(5-fluoro-1H-indol-3-yl)pentanoic acid were obtained (beige solid, m.p. 86–92° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07173045B2 |
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| Source dataset | uspto-grants-2007_02 |
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| ORD ID | ord-c941bde935284000855d28d31531c6c6 |
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| Source note | uspto-grants-2007_02 |
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