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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2199579Generated: October 30, 2026

Ethyl Acetate → HCID 86671864, compound

https://huagongshe.com/reaction/2199579

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantLithium diisopropylamideHCID 2724682—
Reactant2-Bromo-4-methylpyridineHCID 2734087—
Reactant2,3-dihydrothieno[3,4-b][1,4]dioxine-5-carbaldehydeHCID 3540090—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86671864HCID 8667186495%

Reaction Conditions

Temperature-78 °C

Reaction Steps

4-Methyl-2-bromopyridine (450 mg, 2.62 mmol) was dissolved in anhyd THF (10 mL) and the resulting mixture was cooled to −78° C. LDA (1.76 mL, 1.8 M solution in THF, 3.17 mmol) was added dropwise and the resulting mixture was stirred for 1 h at the same temperature. A solution of 3,4-ethylenedioxythiophene-2-carboxaldehyde (500 mg, 2.94 mmol) in THF (20 mL) was added and the resulting mixture was stirred for 30 min at room temperature. AcOEt (120 mL) and water (120 mL) were added and the layers were separated. The organic layer was washed with water (2×150 mL), dried (Na2SO4) and the solvent was removed by rotary evaporation. Flash chromatography of the residue (silica gel, petroleum ether/AcOEt 1:1) afforded (9) as a yellow oil (850 mg, 2.48 mmol, 95%). 1H NMR (500 MHz, CDCl3) δ 8.23 (d, J=5.0 Hz, 1H), 7.38 (s, 1H), 7.10 (d, J=5.0 Hz, 1H), 6.29 (s, 1H), 5.18 (t, J=6.7 Hz, 1H), 4.20-4.05 (m, 4H), 3.20-2.95 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09359334B2
Source datasetuspto-grants-2016_06
ORD IDord-aff1c1e608124d07b89b5700f781cb48
Source noteuspto-grants-2016_06