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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1277532Generated: November 1, 2026

Ethyl formate → rac. 4-Benzyloxy-3-methylbutanal

https://huagongshe.com/reaction/1277532

Reaction equation

Participants

RoleNameHCIDCharge
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. Theresulting 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 250ml. of saturated aqueous ammonium chloride solution. Stirring was continuedfor 20 minutes at which point 125 ml. of 5% by weight aqueous sulfuric acidwas 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 numberUS04277610
Source datasetuspto-grants-1981_07
ORD IDord-ee60592bf1db48539030db9de33a8681
Source noteuspto-grants-1981_07