HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aluminium lithium hydride → (4-Chloro-3-methoxyphenyl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | Methyl 4-chloro-3-methoxybenzoate | HCID 44886974 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (4-Chloro-3-methoxyphenyl)methanol | HCID 10910038 | — |
Reaction Steps
Methyl 4-chloro-3-methoxybenzoate (5 g, 25 mmol, 1 equiv) in 15 mL of THF and 15 mL of DCM was cooled to 0° C. and treated with LiAlH4 (2.8 g, 3 equiv) overnight and was allowed to warm to rt. The reaction was then quenched with saturated sodium sulfate. Removal of the solid by filtration through celite followed by evaporation of the filtrate gave 4-chloro-3-methoxybenzyl alcohol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07576218B2 |
| Source dataset | uspto-grants-2009_08 |
| ORD ID | ord-d3bfbae39385437fa12f5bd6ec78c03d |
| Source note | uspto-grants-2009_08 |