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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1053574Generated: October 27, 2026

Hydroquinone → HCID 71735927, compound

https://huagongshe.com/reaction/1053574

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroquinoneHCID 785—
ReactantPotassium CarbonateHCID 11430—
ReactantN-(3-bromopropyl)-N-methylanilineHCID 61288549—
SolventDimethylformamideHCID 6228—
ProductHCID 71735927HCID 7173592724.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of compound 9a (500 mg, 2.7 mmol), K2CO3 (740 mg, 5.4 mmol), and KI (445 mg, 2.7 mmol) in DMF (50 mL) was bubbled with argon for 10 min Hydroquinone (589 mg, 5.4 mmol) was added to the mixture under argon. The reaction mixture was heated and stirred at 80° C. for 6 hours. After cooling to room temperature, the solvent was evaporated and the residue was quenched with 100 mLs 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 with hexane/EtOAc to provide the compound 9 (170 mg, 0.66 mmol, 24% yield) as a white solid. HRMS (ESI, positive) m/z calcd. for C16H20NO2 [M+H]+: 258.14886, found: 258.14888. 1H NMR (400 MHz, Chloroform-d) δ 7.36-7.27 (m, 2H), 6.94-6.70 (m, 7H), 5.94 (broad s, 1H), 4.00 (t, J=5.9 Hz, 2H), 3.60 (t, J=7.0 Hz, 2H), 3.01 (s, 3H), 2.09 (p, J=6.2 Hz, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394233B2
Source datasetuspto-grants-2016_07
ORD IDord-3ed6e073011b4103a6d62e36e81689fa
Source noteuspto-grants-2016_07