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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2049849Generated: October 29, 2026

Methanol → HCID 13019276, compound

https://huagongshe.com/reaction/2049849

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantHCID 13019275HCID 13019275—
ReactantDiisobutylaluminumhydrideHCID 21225700—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
ProductHCID 13019276HCID 13019276—

Reaction Steps

Di-isobutylaluminum hydride (54 ml., 25% solution in toluene) is added with stirring to a solution of p-hexadecylaminobenzonitrile (11.4 g.) under a nitrogen atmosphere. The temperature rises to 40° C. during the addition which takes 30 minutes, and the reaction is then stirred for 1 hour. A solution of methanol in toluene (50 ml., 1:1) is added over 30 minutes, and the mixture is poured into vigorously stirred ice-cold aqueous sulfuric acid (500 ml., 5%). After 10 minutes diatomaceous earth (30 g.) is added, the mixture filtered and the organic layer separated. The aqueous solution is extracted twice with toluene (100 ml.) and the combined organic layers are washed with aqueous sodium bicarbonate, dried over magnesium sulfate, decolorized with charcoal, filtered and evaporated in vacuo to give a light yellow crystalline solid. The crude product is dissolved in dichloromethane and filtered through magnesium silicate (80 g.) to give a white crystalline material on removal of the solvent. The solid is recrystallized from dichloromethane-hexanes giving p-hexadecylamino benzaldehyde as colorless fine needles (6.0 g.), m.p. 84°-85° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04198522
Source datasetuspto-grants-1980_04
ORD IDord-273c222b0e3b4f4295e4be645b0e2dc8
Source noteuspto-grants-1980_04