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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 929446Generated: October 31, 2026

4-tert-Butylphenol → HCID 89648362, compound

https://huagongshe.com/reaction/929446

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-tert-ButylphenolHCID 7393—
ReactantPotassium CarbonateHCID 11430—
Reactant1,2-Difluoro-4-nitrobenzeneHCID 123053—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 89648362HCID 89648362100%

Reaction Steps

Following procedure A, 3,4-difluoronitrobenzene (401 mg, 2.52 mmol, 1.00 eq) and 4-tert-butylphenol (477 mg, 3.18 mmol, 1.26 eq) were dissolved in DMSO (6 mL). Anhydrous K2CO3 (522 mg, 3.78 mmol, 1.50 eq) was added and the reaction mixture was stirred at room temperature for 19 h. After extraction with Et2O, the crude product was purified by flash column chromatography (SiO2; EtOAc/petrolether 1:50) to afford the title compound as colourless oil (722 mg, 2.52 mmol, 99% yield). Rf=0.54 (EtOAc/PE 1:20). HRMS (ESI) calcd. for C16H17FNO3+ [M+H]+ 290.1187. found: 290.1194. 1H NMR (400 MHz, CDCl3) δ 8.07 (dd, J=10.3, 2.7 Hz, 1H, aromatic H), 7.96 (ddd, J=9.1, 2.7, 1.5 Hz, 1H, aromatic H), 7.49-7.38 (m, 2H, aromatic H), 7.09-6.99 (m, 2H, aromatic H), 6.96 (dd, J=9.1, 8.0 Hz, 1H, aromatic H), 1.35 (s, 9H, C(CH3)3). 13C NMR (101 MHz, CDCl3) δ 153.35, 152.23, 151.93, 151.82, 150.84, 148.70, 142.40, 142.33, 127.29, 120.68, 120.64, 119.38, 117.73, 117.71, 113.28, 113.05, 34.65, 31.54.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296682B2
Source datasetuspto-grants-2016_03
ORD IDord-f959ec4d078a4a1c8b335e724c710f2a
Source noteuspto-grants-2016_03