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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466074Generated: October 30, 2026

Guanidine → HCID 135503589, compound

https://huagongshe.com/reaction/466074

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGuanidineHCID 3520—
ReactantHCID 136401346HCID 136401346—
SolventEthanolHCID 702—
ProductHCID 135503589HCID 135503589—

Reaction Steps

To a solution of 2.6 g (0.044 mole) of guanidine in absolute ethanol (100 ml) is added dropwise a solution of 6.2 g (0.022 mole) of 3,5-bis(1,1-dimethylethyl) -N,4-dihydroxybenzenecarboximidoyl chloride in absolute ethanol (60 ml). The mixture is stirred at room temperature for 18 hours, then evaporated to dryness (vacuum). The oil is dissolved in ethyl acetate (125 ml) and poured into water (125 ml). While stirring, the solution is acidified (pH 4.0-5.0) with 1N hydrochloric acid. The organic layer is separated, washed with water (2×100 ml), and dried (anhydrous magnesium sulfate). Evaporation of the organic layer leaves 5.0 g of crude material. Purification by flash chromatography (silica gel, ethyl acetate/hexane elution) gives 1.0 g (16%) of analytically pure 4-(5-amino-1,2,4-oxadiazol-3-yl)-2,6-bis(1,1-dimethylethyl)phenol, mp 202°-204° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05155122
Source datasetuspto-grants-1992_10
ORD IDord-946d3625dfc84a0eabc4adea9c931b6f
Source noteuspto-grants-1992_10