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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1254400Generated: November 2, 2026

Hydrochloric Acid → 7-Bromo-2-methyl-1-benzofuran

https://huagongshe.com/reaction/1254400

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 numberUS08455521B2
Source datasetuspto-grants-2013_06
ORD IDord-7bbd754d0c784504ada9364a27969f11
Source noteuspto-grants-2013_06