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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1657142Generated: October 30, 2026

2,3-Dihydroxybutanedioic Acid → 4-[(5,6,7,8-Tetrahydro-5,5,8,8-tetramethylnaphth-2-yl)ethynyl]-benzaldehyde

https://huagongshe.com/reaction/1657142

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-Dihydroxybutanedioic AcidHCID 875—
Reactant4-[(5,6,7,8-Tetrahydro-5,5,8,8-tetramethylnaphth-2-yl)ethynyl]-benzonitrileHCID 13604826—
ReactantDiisobutylaluminumhydrideHCID 21225700—
SolventDiethyl EtherHCID 3283—
SolventHexaneHCID 8058—
Product4-[(5,6,7,8-Tetrahydro-5,5,8,8-tetramethylnaphth-2-yl)ethynyl]-benzaldehydeHCID 1978696338%

Reaction Steps

56 ml (67 millimoles) of a 20% strength solution of diisobutylaluminum hydride in hexane were added to a solution of 10 g (32 millimoles) of 4-[(5,6,7,8-tetrahydro- 5,5,8,8-tetramethylnaphth-2-yl)-ethynyl]-benzonitrile (Example 1) in 120 ml of absolute ether. The mixture was stirred for a further 40 minutes, 150 ml of saturated tartaric acid solution were added dropwise and stirring was continued for a further hour. Thereafter, the mixture was extracted three times with ether and the combined ether phases were washed twice with water, dried over Na2SO4 and evaporated down. Recrystallization of the residue from isopropanol gave 3.8 g (38%) of the title compound of melting point 130° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05256694
Source datasetuspto-grants-1993_10
ORD IDord-c4b16abd25bd451ebd72047157bfd36b
Source noteuspto-grants-1993_10