HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2266232Generated: October 30, 2026
Hydrochloric Acid → 7-Bromo-2-methyl-1-benzofuran
https://huagongshe.com/reaction/2266232
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | 7-Bromo-1-benzofuran | HCID 113628 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | Tetrahydrofuran heptane | HCID 21263495 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 7-Bromo-2-methyl-1-benzofuran | HCID 12264721 | 52% |
Reaction Steps
A stirred solution of 7-bromobenzofuran (493 mg, 2.5 mmol) in dry THF (5 mL) was cooled to −70° C. and 2M LDA in 1:1 THF/heptane (1.4 mL, 2.8 mmol) was added dropwise over 2 min. The mixture was stirred at −70° C. for 1 h and methyl iodide (0.19 mL, 3.0 mmol) was added. The mixture was stirred at −70° C. for 3 h and at 0° C. for 1 h. The mixture was poured into 5% aq HCl (60 mL) and extracted with ether (2×50 mL). The combined ether extracts were washed with sat'd aq NaHCO3 (20 mL) and dried over MgSO4. Removal of the solvent left an oil (470 mg) which was purified by chromatography on a 40-g silica cartridge eluted with hexanes to afford 7-bromo-2-methylbenzofuran (277 mg, 52%, estimated purity ˜80%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07858624B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-eb4563c8c3f7406b9b2f432bb22c7c7c |
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| Source note | uspto-grants-2010_12 |
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