HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 18181Generated: October 25, 2026
Sodium Carbonate → 3-Benzyl-7-bromo-5-methyl-benzofuran
https://huagongshe.com/reaction/18181
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Sodium Formate | HCID 2723810 | — |
| Reactant | 1-Bromo-3-iodo-5-methyl-2-(3-phenylallyloxy)-benzene | HCID 68585603 | — |
| Catalyst | Tetrabutylammonium Chloride | HCID 70681 | — |
| Catalyst | Bis(acetonitrile)dichloropalladium | HCID 6093782 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Benzyl-7-bromo-5-methyl-benzofuran | HCID 59344929 | 52.7% |
Reaction Steps
1-Bromo-3-iodo-5-methyl-2-(3-phenylallyloxy)-benzene (10.86 g, 25 mmol), tetrabutylammonium chloride (7.65 gm, 27.5 mmol), sodium carbonate (6.62 g, 62.46 mmol), sodium formate (1.7 g, 25 mmol), and bis(acetonitrile)dichloropalladium(II) (0.467 g, 1.8 mmol) was added to 50 ml DMF. The mixture was degassed and heated under nitrogen at 80° C. for 105 minutes, then cooled to room temperature. Water was added and the mixture was extracted with a hexanes/ethyl acetate (1:1) mixture. The solution was dried onto 20 gm silica gel, the silica gel was layered over 100 gm silica gel in a fritted funnel and eluted with four 400 ml portions of hexanes. The hexanes was removed under reduced pressure to give 3-benzyl-7-bromo-5-methyl-benzofuran (3.97 g, 52% yield). MS: (M+H)+ 302.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07741326B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-7ac7c6a36b2d43f6bce03c300bbc3b33 |
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| Source note | uspto-grants-2010_06 |
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