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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2117233Generated: October 26, 2026

Triglyme → 2-Cyanomethoxy-3-methylbenzylalcohol

https://huagongshe.com/reaction/2117233

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriglymeHCID 8189—
ReactantSodium borohydrideHCID 4311764—
Reactant2-(2-Formyl-6-methylphenoxy)acetonitrileHCID 22241345—
SolventTetrahydrofuranHCID 8028—
Product2-Cyanomethoxy-3-methylbenzylalcoholHCID 22241361—

Reaction Conditions

Temperature0 °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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE040558E1
Source datasetuspto-grants-2008_10
ORD IDord-e84e7450a7ac47cba8f48d97c6fa2cf7
Source noteuspto-grants-2008_10