Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 3989Generated: October 24, 2026

2,3-Dihydroxybutanedioic Acid → 2-[3-[(Phenylethyl)methylamino]-propyl]-2-isopropylphenylacetaldehyde

https://huagongshe.com/en/reaction/3989

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-Dihydroxybutanedioic AcidHCID 875—
ReactantSulfuric AcidHCID 1118—
ReactantPotassium HydroxideHCID 14797—
Reactant5-[Methyl(2-phenylethyl)amino]-2-phenyl-2-propan-2-ylpentanenitrileHCID 71225—
ReactantDiisobutylaluminumhydrideHCID 21225700—
SolventDiethyl EtherHCID 3283—
SolventHexaneHCID 8058—
Product2-[3-[(Phenylethyl)methylamino]-propyl]-2-isopropylphenylacetaldehydeHCID 88638019—

Reaction Steps

180 ml of a 1M solution of diisobutylaluminum hydride in hexane were added dropwise, at -5° C., to a solution of 33.4 g (0.1 mole) of 2-[3-[(phenylethyl)-methylamino]-propyl]-isopropylphenylacetonitrile in 400 ml of diethyl ether. The mixture was stirred for 1.5 hours, after which 500 ml of 10% strength sulfuric acid were added. 30 g of tartaric acid were introduced, the mixture was rendered alkaline with concentrated potassium hydroxide solution, and the ether phase was separated off and washed several times with sodium chloride solution. After the ether phase had been dried over sodium sulfate, the ether was distilled off, the remaining oily residue was dissolved in 300 ml of ethyl acetate, and hydrochloric acid in isopropanol was added. The mixture was left to stand overnight, after which the precipitated hydrochloride was filtered off under suction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04723039
Source datasetuspto-grants-1988_02
ORD IDord-9e27edb996dc4b2e8698c669aeab451a
Source noteuspto-grants-1988_02