HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Indol-1-yl-piperidine-1-carboxylic acid ethyl ester → 1-(1-methyl-piperidin-4-yl)-1H-indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Indol-1-yl-piperidine-1-carboxylic acid ethyl ester | HCID 14090749 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(1-methyl-piperidin-4-yl)-1H-indole | HCID 14090743 | 64.8% |
Reaction Steps
To an ice cooled solution of 4-indol-1-yl-piperidine-1-carboxylic acid ethyl ester (50 g, 0.18 mol) in dry THF (400 mL) was added LAH in small portions (7 g, 0.18 mol). After 2 hours, the mixture was quenched by successive addition of water (7 mL) 15% of sodium hydroxide (7 mL) and water (21 mL). The reaction mixture was filtered. The filtrate was dried and evaporated. The residue crystallized on standing and was recrystallized from a small amount of di-i-propyl ether to give the title compound (25 g, 63% of theory). M.Pt.: 58° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05545636 |
| Source dataset | uspto-grants-1996_08 |
| ORD ID | ord-6fbfa59307b64db5b2d3839a9d5a3d25 |
| Source note | uspto-grants-1996_08 |