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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1390863Generated: November 1, 2026

Sulfuric Acid → rac. 4-Benzyloxy-3-methylbutanal

https://huagongshe.com/reaction/1390863

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantEthyl formateHCID 8025—
ReactantAmmonium ChlorideHCID 25517—
ReactantHydrideHCID 166653—
Reactant4-(Benzyloxy)-3-methylbutanenitrileHCID 10976273—
SolventTolueneHCID 1140—
SolventHexaneHCID 8058—
Productrac. 4-Benzyloxy-3-methylbutanalHCID 14658350—

Reaction Steps

A solution of 5.8 g. (0.0307 mole) of rac. 4-benzyloxy-3-methylbutyronitrile in 290 ml. of hexane was stirred at -65° C. to -70° C. while 22.4 ml. (4.78 g.; 0.0337 mole) of 25% diisobutylaluninum hydride solution in toluene was added dropwise. The resulting solution was stirred at -65° C. to -70° C. for 0.5 hours then at room temperature for 5 hours whereupon 2.8 ml. of ethyl formate was added dropwise. The reaction mixture was then treated with 250 ml. of saturated aqueous ammonium chloride solution. Stirring was continued for 20 minutes at which point 125 ml. of 5% by weight aqueous sulfuric acid was added and stirring was continued for an additional 10 minutes. The organic layer was separated and the aqueous layer was extracted with ether. The organic solutions were combined and processed as in Example 1 giving 4.79 g. (81.3%) of rac. 4-benzyloxy-3-methylbutanal as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04140702
Source datasetuspto-grants-1979_02
ORD IDord-a371355c30c9495b8f1c0f8464d3ad6f
Source noteuspto-grants-1979_02