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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 422150Generated: October 26, 2026

Iodine → 1-Iodo-3,5-bis(propan-2-yloxy)benzene

https://huagongshe.com/reaction/422150

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant1-Bromo-3,5-bis(1-methylethoxy)benzeneHCID 58294815—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product1-Iodo-3,5-bis(propan-2-yloxy)benzeneHCID 5829481679.2%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 1-bromo-3,5-bis(propan-2-yloxy)benzene (46) (2.0 g, 7.3 mmol) in THF (100 mL), cooled to −78° C., a 1.6 M n-BuLi solution in hexanes (9.16 mL, 14.7 mmol) was added dropwise. The temperature was maintained at −78° C. for 30 min, after which a solution of iodine (3.17 g, 29.3 mmol) in THF (15 mL) was added dropwise. The mixture was warmed to −35° C. and maintained at this temperature for 1.5 h. The reaction mixture was diluted with EtOAc (100 mL) and washed with water (2×50 mL) and brine (50 mL). The organic layer was separated, dried (Na2SO4) and concentrated. Purification by column chromatography on silica gel (Hexanes/EtOAc, 4:1) gave 1-iodo-3,5-bis(propan-2-yloxy)benzene (47) (1.85 g, 79%) as a viscous orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101605B2
Source datasetuspto-grants-2012_01
ORD IDord-6818f0183c0d4ae08029564f25499230
Source noteuspto-grants-2012_01