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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1165140Generated: November 1, 2026

3,5-Di-tert-butyl-4-hydroxybenzaldehyde → HCID 135973970, compound

https://huagongshe.com/reaction/1165140

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-Di-tert-butyl-4-hydroxybenzaldehydeHCID 73219—
ReactantHCID 12765428HCID 12765428—
SolventEthanolHCID 702—
ProductHCID 135973970HCID 135973970—

Reaction Steps

0.48 g of 1-aminoimidazole hydrochloride are suspended in 30 ml of ethanol, whereupon 0.93 g of 4-hydroxy-3,5-di-tert.-butylbenzaldehyde is added. The suspension is stirred at room temperature for 3 hours, whereby there results a clear solution which is evaporated in a vacuum. The residue is taken up in 15 ml of water, neutralized (pH=7) with ice-cold saturated sodium bicarbonate solution and extracted rapidly three times with 30 ml of methylene chloride each time. The combined organic phases are dried over sodium sulfate, filtered and evaporated in a vacuum. By sublimation of the residue (160°/12 Torr), there is obtained 1-(4-hydroxy-3,5-di-tert.-butylbenzylideneamino)imidazole of m.p. 171°-174°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04908363
Source datasetuspto-grants-1990_03
ORD IDord-134a66ab3faf4bb59d557d7fb2f1cef1
Source noteuspto-grants-1990_03