HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 3-(7-Chloroquinol-2-ylmethoxy)benzyl alcohol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 3-((7-Chloro-2-quinolinyl)methoxy)benzaldehyde | HCID 19002899 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(7-Chloroquinol-2-ylmethoxy)benzyl alcohol | HCID 19737240 | 102% |
Reaction Steps
The aldehyde of Step 1 (46.64 g, 156.6 mmol) was dissolved in 300 mL of THF. At 0° C., 800 mL of EtOH was added, followed by NaBH4 (5.93 g, 157 mmol). The mixture was then stirred at r.t. (room temperature) for 1 h and poured into cold 25% aq (aqueous) NH4OAc. The organic solvents were evaporated and the title alcohol was extracted with toluene:THF 1:1, dried over Na2SO4 and filtered through silica to yield 47.9 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05266568 |
| Source dataset | uspto-grants-1993_11 |
| ORD ID | ord-c1f2efb795f7473f9cc6fe029ed93581 |
| Source note | uspto-grants-1993_11 |