Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Perchloric Acid | HCID 24247 | — |
| Reactant | HCID 12797238 | HCID 12797238 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 12799968 | HCID 12799968 | 75.3% |
Reaction Steps
A mixture of 2-(n-decyl)indole-6-carboxylic acid (62.5 g), perchloric acid (40 ml of strength 70% w/v) and glacial acetic acid (400 ml) were hydrogenated over palladium on charcoal (5% w/w, 8.0 g) at 80°-90° C. and atmospheric pressure. When hydrogen uptake had ceased (after 4 hours) the hot mixture was filtered and the residue was washed with hot (80° C.) glacial acetic acid (500 ml). The combined filtrates were concentrated in vacuo to 450 ml and were poured onto ice (1000 g). The mixture was adjusted to pH 9 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 solid was collected, was washed with water (3×100 ml) and was dried. The solid was dissolved in boiling ethanol, treated with charcoal, and the solution was filtered. The filtrate was treated with an excess of a solution of hydrogen chloride in ethanol (90 ml of strength 37% w/v) and then the mixture was cooled and diluted with diethyl ether (750 ml). The solid was collected and treated as in Example 56 to give (RS)-2-(n-decyl)indoline-6-carboxylic acid (47.4 g), in the form of a buff solid, m.p. 123°-125° 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-e3aa207f44d7447a97882306b62111c8 |
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| Source note | uspto-grants-1985_01 |
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