HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aluminium lithium hydride → (5-Chloro-1-benzothiophen-2-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | Methyl 5-chloro-1-benzothiophene-2-carboxylate | HCID 23340399 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (5-Chloro-1-benzothiophen-2-yl)methanol | HCID 23340421 | — |
Reaction Steps
To lithium aluminum hydride (26.5 mmol) and 50 ml ether, at -20° under nitrogen, is slowly added methyl 5-chlorobenzothiophene-2-carboxylate (6 g, 26.5 mmol). The mixture is then stirred at -20° for 10 minutes. After no starting material is detectable by thin layer chromatography, the mixture is quenched with 1 ml water, 1 ml 15% NaOH, and 3 ml water at -20°. The mixture is allowed to warm to RT and stirred for 15 hours. The mixture was then filtered and solvent evaporated to give 5-chlorobenzothiophene-2-methanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04224330 |
| Source dataset | uspto-grants-1980_09 |
| ORD ID | ord-fdfe5cd99fe6490e97605364335359ff |
| Source note | uspto-grants-1980_09 |