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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1740514Generated: November 1, 2026

Acetic Acid → Diethyl 2-(5-methoxy-2,3-dihydrobenzofuran-6-yliden)-malonate

https://huagongshe.com/reaction/1740514

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDiethyl MalonateHCID 7761—
ReactantPiperidineHCID 8082—
Reactant5-Methoxy-2,3-dihydrobenzofuran-6-carbaldehydeHCID 10012474—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
ProductDiethyl 2-(5-methoxy-2,3-dihydrobenzofuran-6-yliden)-malonateHCID 69543719—

Reaction Steps

To a solution of 5-Methoxy-2,3-dihydrobenzofuran-6al (295 mg, 1.66 mmol) in benzene was added diethyl malonate (265 mg, 1.66 mmol), acetic acid (20 mL, 0.35 mmol) and piperidine (30 mL, 0.30 mmol). The mixture was heated at reflux for 3 h and then poured into 100 mL of water. This mixture was extracted with three 50 mL portion of ethyl acetate. The combined organic extracts were washed with brine and dried (Na2SO4). Removal of the solvent under reduced pressure gave quatitative yield of the title compound as a yellowish oil: 1H NMR (400 MHz, CDCl3) d 8.02 (s, 1H), 6.79 (s, 1H), 6.78 (s, 1H), 4.52 (t, 2H), 4.30 (m, 4H), 3.80 (s, 3H), 3.18 (t, 2H), 1.28 (m, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05969151
Source datasetuspto-grants-1999_10
ORD IDord-cb8dc08f70e9416380ddd6e7d9b0fcd5
Source noteuspto-grants-1999_10