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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Iodine | HCID 807 | — |
| Reactant | 1,3-Bis(methoxymethoxy)benzene | HCID 12222682 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Iodo-1,3-bis(methoxymethoxy)benzene | HCID 25138787 | 79.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09120774B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-6275d5734b7b4c3da2fe02fdc01e74df |
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| Source note | uspto-grants-2015_09 |
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