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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2204194Generated: November 2, 2026

Dimethylformamide → HCID 58551495, compound

https://huagongshe.com/reaction/2204194

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantIodoethaneHCID 6340—
ReactantCesium carbonateHCID 10796—
ReactantSodium HydroxideHCID 14798—
ReactantBenzoic acid, 2,4-dihydroxy-3-methyl-, methyl esterHCID 118521—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 58551495HCID 5855149580%

Reaction Conditions

Temperature80 °C

Reaction Steps

Methyl 2,4-dihydroxy-3-methyl-benzoate (193 mg, 1.06 mmol) was dissolved in DMF (1 mL) containing cesium carbonate (1.03 g, 3.18 mmol). Iodoethane (847 μL, 10.6 mmol) was added and the reaction mixture was allowed to stir for 86 hours. The reaction mixture was then filtered and evaporated to dryness. The crude material was then dissolved in a mixture of dioxane (2 mL) and sodium hydroxide (1.1 mL of 1.0 M, 1.1 mmol). The reaction mixture was then heated at 80° C. for 75 minutes. The dioxane was evaporated to dryness and the reaction mixture was made acidic with 4M hydrochloric acid. The aqueous layer was extracted 3 times with ethyl acetate. The combined ethyl acetate extracts were then dried over sodium sulfate, filtered, and evaporated to dryness to yield 2,4-diethoxy-3-methyl-benzoic acid (189 mg, 80%) as a pale yellow solid which was used without further purification. 1H NMR (400 MHz, DMSO) δ 12.37 (s, 1H), 7.62 (d, J=8.7 Hz, 1H), 6.79 (d, J=8.8 Hz, 1H), 4.08 (q, J=6.9 Hz, 2H), 3.87 (q, J=7.0 Hz, 2H), 2.06 (s, 3H), 1.36 (t, J=6.9 Hz, 3H), 1.30 (t, J=7.0 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365588B2
Source datasetuspto-grants-2016_06
ORD IDord-f2a8fe6abe4f424e8b7ac892050b7f34
Source noteuspto-grants-2016_06