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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1511226Generated: November 3, 2026

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

https://huagongshe.com/reaction/1511226

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 2 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) 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 numberUS08212011B2
Source datasetuspto-grants-2012_07
ORD IDord-f5d4082b3cb743b3a3951171623f0b26
Source noteuspto-grants-2012_07