HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2244831Generated: November 2, 2026
Iodine → 7,8-Difluoro-5-iodo-6-methoxymethoxychroman
https://huagongshe.com/reaction/2244831
Participants
| Role | Name | HCID | Charge |
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| Reactant | Iodine | HCID 807 | — |
| Reactant | 7,8-Difluoro-6-methoxymethoxychroman | HCID 59215258 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | 7,8-Difluoro-5-iodo-6-methoxymethoxychroman | HCID 59215281 | — |
Reaction Steps
16.6 g (72.1 mmol) of 7,8-difluoro-6-methoxymethoxychroman are initially introduced in 350 ml of THF, and 54.3 ml (86.5 mmol) of n-BuLi (15% soln. in hexane) are added dropwise at −78° C. When the addition is complete, the mixture is stirred at this temperature for 30 min and subsequently at 20° C. for 1 h. The solution is re-cooled to −78° C., and a solution of 22.0 g (86.5 mol) of iodine in 100 ml of THF is added dropwise. The reaction mixture is stirred at room temperature for 1.5 h and subsequently diluted with MTBE. The solution is washed with water and sat. sodium chloride soln. and dried using sodium sulfate. The crude product remaining after removal of the solvents is purified by column chromatography (SiO2, n-heptane:MTBE=2:1), giving 7,8-difluoro-5-iodo-6-methoxymethoxychroman as a brownish oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07678929B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-eb4fe2155ff2426ebb4ccdd6435b6073 |
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| Source note | uspto-grants-2010_03 |
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