HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 5-Bromobiphenyl-2-methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | Methyl 5-bromo-[1,1'-biphenyl]-2-carboxylate | HCID 54332024 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Bromobiphenyl-2-methanol | HCID 117941810 | — |
Reaction Steps
A solution of methyl 5-bromo-[1,1′-biphenyl]-2-carboxylate (2.2 g, 6.9 mmol) in THF (50 mL) was cooled to 0° C. LiAlH4 (380 mg, 10 mmol) was added slowly. The reaction mixture was stirred at RT for 2 h, after which water (1 mL) was added slowly to quench the reaction. The solid was removed by filtration and the filtrate was concentrated in vacuo to provide (5-bromo-[1,1′-biphenyl]-2-yl)methanol as a white solid that was used directly without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09199994B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-d9abe8955b0b490396eface5c0fdf6b8 |
| Source note | uspto-grants-2015_12 |