Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1155846Generated: October 31, 2026

Tetrahydrofuran → 2-(3-(Benzyloxy)phenyl)-2-methylpropanal

https://huagongshe.com/reaction/1155846

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant2-(3-(Benzyloxy)phenyl)-2-methylpropanenitrileHCID 20496863—
ReactantDiisobutylaluminumhydrideHCID 21225700—
SolventHexaneHCID 8058—
Product2-(3-(Benzyloxy)phenyl)-2-methylpropanalHCID 1985535999%

Reaction Steps

To a 15° C. solution of 325 g. (1.25 mole) of 2-(3-benzyloxyphenyl)-2-methylpropionitrile in 1.85 liters of tetrahydrofuran is added 1.6 moles of diisobutylaluminum hydride as a 1.3 M solution in hexane (reaction temperature is maintained at 15°-18° C.). The reaction mixture is allowed to warm to room temperature and is stirred 2 hours longer. It is then quenched by addition to a solution of 170 ml. of concentrated sulfuric acid in 670 ml. of water (temperature ≤30° C.). The resultant mixture is allowed to warm to room temperature and is then stirred an additional 2 hours. The organic layer is separated and the aqueous phase extracted once with one liter of ether. The combined organic phase is washed with 500 ml. of water and 500 ml. of saturated sodium chloride, dried over magnesium sulfate and evaporated to yield 315 g. (99%) of the title product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04332942
Source datasetuspto-grants-1982_06
ORD IDord-9a837b4387e1421d95db2bd7d2eb3da7
Source noteuspto-grants-1982_06