HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2412598Generated: November 2, 2026
Tetrafluoroboric acid → HCID 12799964, compound
https://huagongshe.com/reaction/2412598
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrafluoroboric acid | HCID 28118 | — |
| Reactant | HCID 12797216 | HCID 12797216 | — |
| Catalyst | Platinum oxide (PtO) | HCID 82844 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 12799964 | HCID 12799964 | 45.4% |
Reaction Steps
2-(n-Pentadecyl)indole-6-carboxylic acid (16.0 g) was dissolved in a mixture of tetrahydrofuran (400 ml) and ethanol (100 ml), containing aqueous fluoroboric acid (100 ml, of strength 40% w/v). The stirred mixture was hydrogenated over platinum oxide (2.0 g) at room temperature and atmospheric pressure. After 6 hours the mixture was filtered, the residue was washed with diethyl ether (100 ml) and the combined filtrates were concentrated in vacuo until a solid separated. The mixture was adjusted to pH 7 by treatment with an aqueous solution of sodium hydroxide (strength 50% w/v) and was then adjusted to pH 4-5 with glacial acetic acid. The mixture was extracted with diethyl ether (3×100 ml), and the ether solution was dried over magnesium sulphate and, on evaporation in vacuo, gave a solid. The solid was recrystallised from a mixture of toluene and hexane (equal parts by volume) to give (RS)-2-(n-pentadecyl)-indoline-6-carboxylic acid (7.3 g), in the form of a colourless solid, m.p. 119°-122° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04493843 |
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| Source dataset | uspto-grants-1985_01 |
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| ORD ID | ord-6a0158bbec014d7a8b04b7d67aa89549 |
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| Source note | uspto-grants-1985_01 |
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