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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Iodine | HCID 807 | — |
| Reactant | 1-Bromo-3,5-bis(1-methylethoxy)benzene | HCID 58294815 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-Iodo-3,5-bis(propan-2-yloxy)benzene | HCID 58294816 | 79.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08101605B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-6818f0183c0d4ae08029564f25499230 |
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| Source note | uspto-grants-2012_01 |
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