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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 402784Generated: October 26, 2026

Water → 4,4-dimethyl-8-(propan-2-yl)-3,4-dihydro-2H-chromene-6-carbaldehyde

https://huagongshe.com/reaction/402784

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDimethylformamideHCID 6228—
Reactant6-bromo-4,4-dimethyl-8-(propan-2-yl)-3,4-dihydro-2H-chromeneHCID 45255972—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product4,4-dimethyl-8-(propan-2-yl)-3,4-dihydro-2H-chromene-6-carbaldehydeHCID 77230776—

Reaction Conditions

Temperature-78 °C

Reaction Steps

6-Bromo-4,4-dimethyl-8-(propan-2-yl)-3,4-dihydro-2H-chromene (154 mg, 0.54 mmol) in tetrahydrofuran (5.44 mL) was cooled to −78° C. and n-BuLi (261 μL, 0.65 mmol) was added dropwise via a syringe. The reaction mixture was stirred at −78° C. for 30 minutes, and then DMF (168 μL, 2.17 mmol) was added dropwise. The resulting mixture was allowed to warm to room temperature, and stirred for 30 minutes before water was added. It was then extracted with EtOAc (2×) and the combined organic layers were dried over Na2SO4, filtered, and concentrated under vacuum. The crude residue was purified by silica gel chromatography eluting with 0-10% EtOAc/Hexanes to obtain the desired product as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08742110B2
Source datasetuspto-grants-2014_06
ORD IDord-1d3fe5d735954dee874792b29cde22b3
Source noteuspto-grants-2014_06