HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium triethylborohydride → (3-Bromo-2-chlorophenyl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium triethylborohydride | HCID 23712863 | — |
| Reactant | Methyl 3-bromo-2-chlorobenzoate | HCID 67516858 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (3-Bromo-2-chlorophenyl)methanol | HCID 67146654 | — |
Reaction Steps
To a solution of methyl 3-bromo-2-chlorobenzoate (1.9 g, 7.6 mmol) in THF (30 mL) was added Super Hydride (23 mL, 23 mmol) at 0° C. The reaction was allowed to stir for 16 hours. The reaction was diluted with EtOAc, washed with brine, dried over sodium sulfate, and purified by MPLC to provide (3-bromo-2-chlorophenyl)methanol. LC-MS (IE, m/z): 205 [M−17]+;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08999991B2 |
| Source dataset | uspto-grants-2015_04 |
| ORD ID | ord-efa4b3f766694e9b98ad645a2fa9227e |
| Source note | uspto-grants-2015_04 |