HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium sulfate decahydrate → 2-(5-chloro-3-methylsulfanyl-1H-indol-2-yl)-ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium sulfate decahydrate | HCID 62649 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | (5-chloro-3-methylsulfanyl-1H-indol-2-yl)-acetic acid methyl ester | HCID 69545956 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-(5-chloro-3-methylsulfanyl-1H-indol-2-yl)-ethanol | HCID 22574103 | — |
Reaction Steps
To a solution of (5-chloro-3-methylsulfanyl-1H-indol-2-yl)-acetic acid methyl ester (0.252 g, 0.93 mmole) in ether (10 ml) was added 0.93 ml of a 1M solution of lithium aluminum hydride in ether at room temperature. The reaction mixture was stirred for 15 minutes, after which time sodium sulfate decahydrate (1 g) was cautiously added. The reaction mixture was stirred for an hour at room temperature, filtered, and the filtrate evaporated to dryness. The crude alcohol was purified by column chromatography (silica gel) using 7:3 hexane:ethyl acetate as the eluting solvent. The pure 2-(5-chloro-3-methylsulfanyl-1H-indol-2-yl)-ethanol was isolated as a pale solid (0.191 g, 84% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06852726B2 |
| Source dataset | uspto-grants-2005_02 |
| ORD ID | ord-a4e26d10e9de41e7b1672cfefe6736c6 |
| Source note | uspto-grants-2005_02 |