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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 460291Generated: October 27, 2026

Water → 3,3-Dimethyl-2,3-dihydrobenzofuran-5-carbaldehyde

https://huagongshe.com/reaction/460291

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDimethylformamideHCID 6228—
Reactant5-Bromo-3,3-dimethyl-2,3-dihydro-1-benzofuranHCID 5323595—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product3,3-Dimethyl-2,3-dihydrobenzofuran-5-carbaldehydeHCID 20536180106.6%

Reaction Conditions

Temperature-50 °C

Reaction Steps

To a solution of 5-bromo-3,3-dimethyl-2,3-dihydro-benzofuran (example 1f) (15.90 g, 70.01 mmol) in dry THF (100 mL) at −78° C., under argon, was added dropwise n-BuLi (1.6 M in hexane, 105 mmol, 42 mL). The mixture was stirred for 5 minutes then DMF (16.3 mL, 210 mmol) was added and the mixture was quickly warmed up to −50° C. and then to 0° C. for 3 hrs. Water was added slowly and the solution extracted with ethyl acetate. The organic layer was further washed with water, brine, dried (MgSO4), filtered and evaporated to give 13.15 g of 3,3-dimethyl-2,3-dihydro-benzofuran-5-carbaldehyde use as this in the next step. 1H NMR (300 MHz; CDCl3): 1.38 (s, 6H), 4.36 (s, 2H), 6.89 (d, J=7.8 Hz, 1H), 7.68 (m, 2H), 9.85 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07196108B2
Source datasetuspto-grants-2007_03
ORD IDord-e8f04aa31ae343e294a11c76eddf8085
Source noteuspto-grants-2007_03