HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium borohydride → (2-Fluoro-3-morpholinophenyl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | 2-(2-Bromoethoxy)ethyl 2-fluoro-3-morpholinobenzoate | HCID 66765171 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2-Fluoro-3-morpholinophenyl)methanol | HCID 66765145 | — |
Reaction Steps
To a solution of 2-(2-bromoethoxy)ethyl 2-fluoro-3-morpholinobenzoate (450 mg, 1.2 mmol) in THF (5 mL) was added lithium borohydride (1.5 eq) and the reaction stirred at rt for 18 h. The reaction was quenched by addition of saturated NH4Cl (aq) and extracted with EtOAc. The organic phase was dried (Na2SO4), filtered and concentrated in vacuo. The resultant residue was purified by column chromatography (petroleum ether: EtOAc) to give (2-fluoro-3-morpholinophenyl)methanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09040545B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-5e1b829888cb42a3be37cfd3f8ef5800 |
| Source note | uspto-grants-2015_05 |