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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2415238Generated: November 1, 2026

4-Aminophenol → HCID 22641092, compound

https://huagongshe.com/reaction/2415238

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AminophenolHCID 403—
ReactantWaterHCID 962—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
ReactantHCID 10787760HCID 10787760—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 22641092HCID 2264109265%

Reaction Steps

A solution of 250 mg (0.63 mmol) of 4-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-2-naphthylselanylethynyl)benzoic acid obtained in Example 5, 169 mg (1.25 mmol) of 1-hydroxybenzoctriazole, 240 mg (1.25 mmol) of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide (EDC) and 82 mg (0.75 mmol) of 4-aminophenol in 20 ml of THF is stirred at room temperature for 15 h. Water and ethyl acetate are then added. After stirring and separation of the phases by settling, the aqueous phase is extracted with ethyl acetate. The organic phases are then combined and washed with water, dried over magnesium sulphate and concentrated on a rotary evaporator under vacuum at 40° C. The product is purified on a column of silica (ethyl acetate 20/heptane 80). 200 mg (65%) of a white solid are obtained. m.p.=202° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06818666B2
Source datasetuspto-grants-2004_11
ORD IDord-9f0fbe7b9fda432e91ec8ce463cd3990
Source noteuspto-grants-2004_11