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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 460290Generated: October 29, 2026

Hydrochloric Acid → 7-Bromo-3,3-dimethyl-2,3-dihydro-benzofuran-5-carbaldehyde

https://huagongshe.com/reaction/460290

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBromineHCID 24408—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant3,3-Dimethyl-2,3-dihydrobenzofuran-5-carbaldehydeHCID 20536180—
SolventDichloromethaneHCID 6344—
Product7-Bromo-3,3-dimethyl-2,3-dihydro-benzofuran-5-carbaldehydeHCID 1844542291.4%

Reaction Steps

To a solution of AlCl3 (1.22 g, 9.18 mmol) in dry dichloromethane (15 mL) was added dropwise at room temperature 3,3-dimethyl-2,3-dihydro-benzofuran-5-carbaldehyde (647 mg, 3.67 mmol) in dichloromethane (15 mL) followed by bromine (0.23 mL, 4.41 mmol) and the reaction stirred for 3 hours. 1N HCl was added slowly and the layers separated. The aqueous layer was extracted twice with dichloromethane. The combined organic layers were washed successively with water and brine, dried over anhydrous magnesium sulfate, filtered and evaporated. The residue was chromatographed on silica gel (20% ethyl acetate in hexane) to give 856 mg of 7-bromo-3,3-dimethyl-2,3-dihydro-benzofuran-5-carbaldehyde (91%). 1H NMR (300 MHz; CDCl3): 1.40(s, 6H), 4.46 (s, 2H), 7.61 (s, 1H), 7.83 (s, 1H), 9.80 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07196108B2
Source datasetuspto-grants-2007_03
ORD IDord-ed79324e1e1940d88aefca98ea74b8f3
Source noteuspto-grants-2007_03