HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 322981Generated: October 27, 2026
Methyl iodide → 2-(5-Methoxy-2-methylphenyl)-[1,3]dioxolane
https://huagongshe.com/reaction/322981
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | 1,3-Dioxolane, 2-(2-bromo-5-methoxyphenyl)- | HCID 11184503 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(5-Methoxy-2-methylphenyl)-[1,3]dioxolane | HCID 22171233 | — |
Reaction Steps
A stirred solution of 2-(2-bromo-5-methoxyphenyl)-[1,3]dioxolane (25.92 g) in tetrahydrofuran (400 mL) at −70° C. is treated dropwise with a solution of n-butyl lithium in hexanes (48.0 mL, 2.5 M). After stirring for 10 minutes methyl iodide (21.29 g) is added dropwise whilst maintaining the temperature at −65° C. The reaction mixture is stirred at −65° C. for 1 hour, allowed to warm to room temperature and stirring is continued for a further hour. The reaction mixture is evaporated and the residue partitioned between ethyl acetate (50 mL) and water (50 mL). The organic phase is washed with brine (500 mL),dried over magnesium sulphate and evaporated to give 2-(5-methoxy-2-methyl-phenyl)-[1,3]dioxolane (18.25 g) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06211234B1 |
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| Source dataset | uspto-grants-2001_04 |
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| ORD ID | ord-82e3fcedf4dd42e0803a1b9eea3c4cc5 |
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| Source note | uspto-grants-2001_04 |
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