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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1390901Generated: October 31, 2026

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

https://huagongshe.com/reaction/1390901

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantEthyl formateHCID 8025—
ReactantAmmonium ChlorideHCID 25517—
Reactant4-(Benzyloxy)-3-methylbutanenitrileHCID 10976273—
ReactantDiisobutylaluminumhydrideHCID 21225700—
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% diisobutylaluminum 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 numberUS04140723
Source datasetuspto-grants-1979_02
ORD IDord-9bb9c4a4d7b2432c99f0fdd6c31d255c
Source noteuspto-grants-1979_02