HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2261108Generated: October 25, 2026
Water → 5-(1,3-Dioxolan-2-yl)-2-methylbenzofuran
https://huagongshe.com/reaction/2261108
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | 5-(1,3-Dioxolan-2-yl)-1-benzofuran | HCID 55255325 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-(1,3-Dioxolan-2-yl)-2-methylbenzofuran | HCID 57469676 | 70% |
Reaction Steps
5-[1,3]Dioxolan-2-yl-benzofuran (50 mg, 0.26 mmol) was dissolved in THF (2 mL) and the solution was cooled down to −78° C. Butyl lithium (180 uL, 1.1 eq.) was added dropwise. This mixture was stirred 30 min at 25° C. Then the reaction mixture was cooled down to −78° C. and iodomethane (18.1 uL, 1.1 eq.) dissolved in 1 mL THF was added dropwise to the reaction mixture. The temperature was increased slowly to room temperature overnight. Despite some starting material was detected, water and ethyl acetate were added to the mixture and the aqueous layer was extracted 3 times. Combined organic phases was dried over MgSO4, filtrated and evaporated to give 2-methyl-5-[1,3]dioxolan-2-yl-benzofuran (41.2 mg, 70%) sufficiently pure to be used in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07846925B2 |
|---|
| Source dataset | uspto-grants-2010_12 |
|---|
| ORD ID | ord-d4dfb744593846dfa53119146824ee3a |
|---|
| Source note | uspto-grants-2010_12 |
|---|