HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triglyme → 2-Cyanomethoxy-3-methylbenzylalcohol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triglyme | HCID 8189 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-(2-Formyl-6-methylphenoxy)acetonitrile | HCID 22241345 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Cyanomethoxy-3-methylbenzylalcohol | HCID 22241361 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
A 2M triglyme solution of sodium borohydride (16.0 mL, 32.1 mmoles) is slowly added to a cooled (−78° C.) solution of 2-cyanomethoxy-3-methylbenzaldehyde (11.25 g, 64.2 mmoles) in THF (180 mL). After stirring for one hour, the reaction is warmed to 0° C. for two hours, then quenched with 2N HCl (16.8 mL) and diluted with ether. The organic layer is isolated and washed with twice with distilled water and brine, then dried over MgSO4. The organic solution is concentrated to give the title compound as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06635655B1 |
| Source dataset | uspto-grants-2003_10 |
| ORD ID | ord-f9ae5007515942708bf2ec8bceeb1090 |
| Source note | uspto-grants-2003_10 |