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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1033846Generated: October 31, 2026

Methanol → HCID 590599, compound

https://huagongshe.com/reaction/1033846

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSulfuric AcidHCID 1118—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 19024953HCID 19024953—
ReactantDiisobutylaluminumhydrideHCID 21225700—
SolventTolueneHCID 1140—
ProductHCID 590599HCID 590599—

Reaction Steps

Under an argon atmosphere, a 500 ml round-bottomed flask was charged with 140 ml of a toluene solution of 4.6 g (33 mmol) of the diethyl 2-methylterephthalonitrile, and further, 87 ml of a toluene solution of 18.6 g (131 mmol) of diisobutylaluminum hydride was added dropwise at -78° C. The resultant mixture was stirred for 30 minutes as it was, and then allowed to further react at room temperature for 5 hours. While the reaction mixture was hot, 4 ml of methanol was added to decompose an excess amount of the diisobutylaluminum hydride. Thereafter, the reaction mixture was poured into 250 ml of a saturated ammonium chloride aqueous solution, and the resultant mixture was stirred at room temperature for 20 minutes. The reaction mixture was recharged into a separating funnel, 100 ml of 10% sulfuric acid was added, and the resultant mixture was shaken vigorously. And, an organic layer formed was separated. This organic layer was washed with sodium bicarbonate and salt water, and dried over magnesium sulfate. The solvent was distilled off with a rotary evaporator, and the residue was purified by column chromatography to give 2.8 g (19 mmol) of 2-methylterephthalaldehyde.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05312913
Source datasetuspto-grants-1994_05
ORD IDord-8da2d00685834c159bfbd29bb9b316d2
Source noteuspto-grants-1994_05