HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aluminium lithium hydride → (1-(4-Bromophenyl)cyclopropyl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | Ethyl 1-(4-bromophenyl)cyclopropanecarboxylate | HCID 53216840 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (1-(4-Bromophenyl)cyclopropyl)methanol | HCID 20252945 | — |
Reaction Steps
To 1-(4-bromo-phenyl)-cyclopropanecarboxylic acid ethyl ester (10.0 g, 37.2 mmol) in THF (100 mL) at 0° C. was added lithium aluminum hydride (2.11 g, 55.7 mmol) and the reaction was stirred for 1 hour at room temperature. The mixture was quenched with H2O (2 mL), followed by 4 N aqueous NaOH (2 mL) and additional H2O (6 mL). After stirring for 15 minutes, the solid precipitate was removed by filtration and the filtrate was concentrated and dried to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09090573B2 |
| Source dataset | uspto-grants-2015_07 |
| ORD ID | ord-7ac50cbef6494b6b8fe5bb383f4cff32 |
| Source note | uspto-grants-2015_07 |