Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1362312Generated: October 27, 2026

2-Iodophenol → 1-But-2-enyloxy-iodobenzene

https://huagongshe.com/reaction/1362312

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-IodophenolHCID 10784—
ReactantSodium hydrideHCID 24758—
Reactant2-Butene, 1-bromo-HCID 122414—
SolventDimethylformamideHCID 6228—
Product1-But-2-enyloxy-iodobenzeneHCID 6140005899%

Reaction Steps

An ice-cold solution of 2-iodophenol (10.0 g, 45.4 mmol) in DMF (100 mL) was added dropwise to a solution of NaH (2.16 g, 90.8 mmol) in DMF at 0° C. Crotylbromide (7.97 g, 59.0 mmol) was then added. The mixture was warmed to room temperature and stirred overnight. The reaction was quenched with water (50 mL) and the mixture was extracted with CH2Cl2 (3×). The combined organics were washed with brine and dried over Na2SO4 to give the title compound (12.2 g, 99%) as a yellow oil: 1H NMR (500 MHz, DMSO-d6) δ 7.76 (dd, J=7.8, 1.5 Hz, 1H), 7.27-7.22 (m, 1H), 6.80 (dd, J=8.4, 1.2 Hz, 1H), 6.70-6.65 (m, 1H), 5.95-5.80 (m, 1H), 5.75-5.65 (m, 1H), 4.55-4.45 (m, 2H), 1.76-1.70 (m, 3H); ESI MS m/z 275 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879872B2
Source datasetuspto-grants-2011_02
ORD IDord-1d9f9805d24a4b2dbe74d73868aec59e
Source noteuspto-grants-2011_02