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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1053563Generated: November 1, 2026

Hydroquinone → HCID 71613318, compound

https://huagongshe.com/reaction/1053563

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroquinoneHCID 785—
ReactantPotassium CarbonateHCID 11430—
ReactantN-(2-Chloroethyl)-N-(propan-2-yl)anilineHCID 13955455—
SolventDimethylformamideHCID 6228—
ProductHCID 71613318HCID 7161331838.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of compound 4c (400 mg, 2 mmol), K2CO3 (558 mg, 4 mmol), and KI (720 mg, 4 mmol) in DMF (50 mL) was bubbled with argon for 10 min Hydroquinone (440 mg, 4 mmol) was added to the mixture under argon. The reaction mixture was heated and stirred at 80° C. for 6 hr. After cooling to room temperature, the solvent was evaporated and the residue was quenched with 100 mL water. The mixture was adjusted pH to ˜7 with diluted hydrochloric acid. The mixture was then extracted with CH2Cl2 and the combined organic layer was washed with water and then brine and was dried over Na2SO4. The solvent was evaporated and the residue was purified by silica gel column chromatography to provide compound 4 (210 mg, 0.77 mmol, 38.3% yield) as a brown oil. HRMS (ESI, positive) m/z calcd. for C17H22N1O2 [M+H]+: 272.16451, found: 272.16455. 1H NMR (400 MHz, CDCl3) δ 7.16-7.05 (m, 2H), 6.75-6.56 (m, 7H), 4.08-3.83 (m, 4H), 3.50-3.42 (t, J=7.1 Hz, 1H), 1.19-1.06 (m, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394233B2
Source datasetuspto-grants-2016_07
ORD IDord-d5121d14fb004e87804c8dff5ae7118f
Source noteuspto-grants-2016_07