Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2272781Generated: November 3, 2026

Iodine → 2-Iodo-1,3-bis(methoxymethoxy)benzene

https://huagongshe.com/reaction/2272781

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant1,3-Bis(methoxymethoxy)benzeneHCID 12222682—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product2-Iodo-1,3-bis(methoxymethoxy)benzeneHCID 2513878779.6%

Reaction Steps

n-Butyllithium (2.5 M in hexanes, 0.22 mL, 0.56 mmol) was added to a solution of 12 (100 mg, 0.50 mmol) in anhydrous THF (790 μL) at 0° C. After 5 minutes, iodine (141 mg, 0.56 mmol) in anhydrous THF (320 μL) was added. After two hours at room temperature, the reaction was quenched via dropwise addition of MeOH and the solvent was concentrated. Water (5 mL) was added and the solution was extracted with EtOAc (3×10 mL). Combined organics were washed with saturated aqueous Na2S2O3, saturated aqueous NaCl, dried (Na2SO4), filtered, and concentrated to afford 15 as a brown oil (129 mg, 79%): 1H NMR (CDCl3, 100 MHz) δ 7.25-7.18 (m, 1H), 6.79-6.71 (m, 2H), 5.27 (s, 2H), 5.18 (s, 2H), 3.54 (s, 3H), 3.50 (s, 3H); IR (film) νmax 2953, 2924, 2853, 1458, 1377 cm−1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120774B2
Source datasetuspto-grants-2015_09
ORD IDord-6275d5734b7b4c3da2fe02fdc01e74df
Source noteuspto-grants-2015_09