HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1195278Generated: November 3, 2026
Methanol → 5-(2-Benzyloxyethyl)-6-methyl-1,3-benzodioxole
https://huagongshe.com/reaction/1195278
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | HCID 19001633 | HCID 19001633 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 5-(2-Benzyloxyethyl)-6-methyl-1,3-benzodioxole | HCID 19001663 | — |
Reaction Steps
3.0 g of 5-(2-benzyloxyethyl)-6-bromo-1,3-benzodioxole was dissolved in 100 m(of anhydrous ether. 8.5 ml of a 1.6 M solution of n-butyllithium in hexane was added to the solution at -78° C. and the reaction was conducted at -50° C. for 2 h. The reaction mixture was cooled again to -78° C. 6.4 g of methyl iodide was added thereto and the temperature was gradually elevated to room temperature. Methanol and water were added to the reaction mixture. After extraction with ethyl acetate, the extract was dried over magnesium sulfate and concentrated under reduced pressure to obtain a crude methyl compound. After purification according to silica gel column chromatography (ethyl acetate/ hexane=2:98), 1.9 g of the intended compound was obtained in the form of a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05110956 |
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| Source dataset | uspto-grants-1992_05 |
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| ORD ID | ord-cff42e49f36945b790603d9208912868 |
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| Source note | uspto-grants-1992_05 |
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