HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl 4-(indol-3-yl)butyrate → 4-(1H-indol-3-yl)butan-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl 4-(indol-3-yl)butyrate | HCID 85010 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(1H-indol-3-yl)butan-1-ol | HCID 11171478 | 107% |
Reaction Steps
A tetrahydroturan solution (500 ml) of methyl 4-(3-indolyl)-butyrate (103 g) was added dropwise to a suspension of lithium aluminium hydride (25 g) in tetrahydrofuran (1000 ml) at 40° C. followed by stirring for 1 h at room temperature. Usual work-up gave 4-(3-indolyl)-1-butanol (96 g) as an oil. Arylation with 1-fluoro-4-iodobenzene according to the method described in EXAMPLE 5 yielded 4-[1-[4-fluorophenyl)-3-indolyl]-1-butanol which was converted to the title compound 9a by the method described in EXAMPLE 2 using spiro[1H-2-benzopyran-4(3H),4'-piperidine]. The maleate salt crystallized from acetone by addition of maleic acid. Yield: 1.5 g, mp: 189°-90° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05807871 |
| Source dataset | uspto-grants-1998_09 |
| ORD ID | ord-118ac1b19e8e4e869ffb822c6cc31296 |
| Source note | uspto-grants-1998_09 |