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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethyl iodideHCID 6328—
Reactant7-Bromo-1-benzofuranHCID 113628—
ReactantLithium diisopropylamideHCID 2724682—
ReactantTetrahydrofuran heptaneHCID 21263495—
SolventTetrahydrofuranHCID 8028—
Product7-Bromo-2-methyl-1-benzofuranHCID 1226472152%

Reaction Conditions

Temperature-70 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858624B2
Source datasetuspto-grants-2010_12
ORD IDord-eb4563c8c3f7406b9b2f432bb22c7c7c
Source noteuspto-grants-2010_12