Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 1,3-Propanediol | HCID 10442 | — |
| Reactant | HCID 22012240 | HCID 22012240 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 15390685 | HCID 15390685 | — |
Reaction Steps
A mixture of 3-acetyloxy-1-phenylindole (24 g), 1,3-dihydroxypropane (240 ml), and conc. sulfuric acid (10 ml) was heated to 80° C. for 2 h. Water was added followed by extraction with ether. The ether phase was dried over magnesium sulfate followed by removal of solvent in vacuo giving 3-(1-phenyl-3-indolyloxy)-1-propanol, sufficiently pure for use in the next step. The title compound was obtained by the method described in EXAMPLE 2 using spiro[isobenzofuran-1(3H),4'-piperidine] and crystallized as the oxalate salt from acetone by addition of oxalic acid. Yield: 2 g, mp: 151°-54° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05665725 |
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| Source dataset | uspto-grants-1997_09 |
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| ORD ID | ord-a5e9fb4f8bb14a75922094d4aef9c405 |
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| Source note | uspto-grants-1997_09 |
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