HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl 3-bromo-5-methoxybenzoate → (3-Bromo-5-methoxyphenyl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl 3-bromo-5-methoxybenzoate | HCID 15618226 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (3-Bromo-5-methoxyphenyl)methanol | HCID 10608788 | — |
Reaction Steps
13.5 Grams (55 mmole)) Methyl 3-bromo-5-methoxybenzoate was dissolved in ether and cooled in an ice bath. 33 ml of 1M lithium aluminum hydride was added dropwise. The reaction mix was then quenched cautiously by addition of sodium sulfate decahydrate, then water, and solid residue was removed by filtration. The ether was separated and evaporated under reduced pressure to give 11 gms of 3-bromo-5-methoxy benzyl alcohol as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06943169B2 |
| Source dataset | uspto-grants-2005_09 |
| ORD ID | ord-af9cce0085bd4ffeae37d5840c90d210 |
| Source note | uspto-grants-2005_09 |