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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1176162Generated: October 31, 2026

1-Bromododecane → Benzene, 1-(dodecyloxy)-4-iodo-

https://huagongshe.com/reaction/1176162

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BromododecaneHCID 8919—
Reactant4-IodophenolHCID 10894—
ReactantPotassium CarbonateHCID 11430—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductBenzene, 1-(dodecyloxy)-4-iodo-HCID 10883601—

Reaction Steps

4-Iodophenol (3.03 g, 1.38×10−2 mol), 1-bromododecane (6.65 ml, 2.77×10−2 mol) and K2CO3 (3.81 g, 2.76×10−2 mol) were dissolved in 50 ml of dry DMF and refluxed for 3.5 h under N2. After cooling, the solution was diluted with water, 2M HCl, and extracted with CH2Cl2. The combined organic layers were washed with saturated aq. NaHCO3, water, and dried over Na2SO4. The product was chromatographed on silica gel with 3:1 hexane:CHCl3 as the eluent. Yield=5.274 g (98% based on 3.03 g of 4-iodophenol). 1H NMR (250 MHz, CDCl3): δ 7.53 (d, 2H, J=8.8 Hz, Ph), 6.67 (d, 2H, J=9.0 Hz, Ph), 3.90 (t, 2H, J=6.5 Hz, —OCH2—), 1.76 (quint, 2H, J=6.6 Hz, —OCH2CH2—), 1.13-1.48 (m, 18H, —CH2—), 0.88 (t, 3H, J=6.4 Hz, —CH3). CI MS m/z: 388.125 (M+) (calcd 388.126).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842758B2
Source datasetuspto-grants-2010_11
ORD IDord-d65d56decee546a287c7f166d46f3aaa
Source noteuspto-grants-2010_11