Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1796596Generated: November 2, 2026

(4-Aminophenoxy)benzene → HCID 21025113, compound

https://huagongshe.com/reaction/1796596

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Aminophenoxy)benzeneHCID 8764—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 21025099HCID 21025099—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 21025113HCID 2102511376%

Reaction Steps

To a solution of compound 1D (26 mg, 0.10 mmol) in DMF (2 mL) were added K2CO3 (138 mg, 1.00 mmol) and p-phenoxyaniline (20 mg, 0.11 mmol) at 25° C. The reaction mixture was stirred for 12 h and then diluted with dichloromethane (15 mL) and washed with water (10 mL) and brine (10 mL). The organic phase was dried over Na2SO4 and concentrated and the resulting residue was triturated with methanol to afford 31 mg (76% yield) of the desired compound as a yellow solid. HPLC: 100% at 4.62 min (retention time) (YMC S5 ODS column, 4.6×50 mm, eluting with 10-90% aqueous methanol over 4 min containing 0.2% phosphoric acid, 4 mL/min, monitoring at 220 nm). MS (ES): m/z 413.12 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07030112B2
Source datasetuspto-grants-2006_04
ORD IDord-6e264df2306845b7a5cdf27995abbd15
Source noteuspto-grants-2006_04