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. TLC showed clean reaction. The reaction was diluted with EtOAc, washed with brine, dried over sodium sulfate, and purified by MPLC to furnish (3-bromo-2-chlorophenyl)methariol. LC-MS (IE, m/z): 205 [M-17]+;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09056859B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-70e472bf31484c2aa72e804ef4cf7dd7 |
| Source note | uspto-grants-2015_06 |