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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1790209Generated: November 1, 2026

Water → 5-Isobutyl-3,3-dimethyl-2,3-dihydro-benzofuran

https://huagongshe.com/reaction/1790209

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTrifluoroacetic acidHCID 6422—
ReactantTriethylsilaneHCID 12052—
Reactant1-(3,3-Dimethyl-2,3-dihydrobenzofuran-5-yl)-2-methyl-propan-1-olHCID 22041408—
SolventDichloromethaneHCID 6344—
Product5-Isobutyl-3,3-dimethyl-2,3-dihydro-benzofuranHCID 2204139787.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a cold solution (0° C.) of 1-(3,3-dimethyl-2,3-dihydro-benzofuran-5-yl)-2-methyl-propan-1-ol (1.97 g, 8.93 mmol) in dry dichloromethane (40 mL) was added triethylsilane (2.85 mL, 17.86 mmol). After 10 minutes, trifluoroacetic acid was the reaction mixture stirred at 0° C. for 30 minutes. Water was poured into the reaction mixture and the layers separated. The organic layer was further washed with water, aqueous NaHCO3 and brine, dried (Mg2SO4), filtered and evaporated. The residue was purified on silica gel (0% to 5% ethyl acetate in hexane) to give 1.6 g of 5-isobutyl-3,3-dimethyl-2,3-dihydro-benzofuran (87%). 1H NMR (300 MHz; CDCl3): δ 0.90 (d, J=6.3 Hz, 6 H), 1.32 (s, 6 H), 1.79 (m, 1 H), 2.40 (d, J=6.9 Hz, 2 H), 4.20 (s, 2 H), 6.68 (dd, J=1.2 Hz and 7.5 Hz, 1 H), 6.87 (m, 2 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07071218B2
Source datasetuspto-grants-2006_07
ORD IDord-901ce828923d41e8b5486673c213dff6
Source noteuspto-grants-2006_07