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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2055760Generated: November 1, 2026

Dimethylformamide → HCID 58788081, compound

https://huagongshe.com/reaction/2055760

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant1-BromododecaneHCID 8919—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 3,5-DihydroxybenzoateHCID 75076—
SolventWaterHCID 962—
ProductHCID 58788081HCID 58788081—

Reaction Steps

In a 1 L RBF containing a stir bar and DMF (100 mL); methyl 3,5-dihydroxylbenzoate (20 g, 0.1190 M), potassium carbonate (49.34 g, 0.3570 M), 1-bromododecane (57.2 mL, 0.2380 M) and DMF (100 mL) were added. The reaction mixture was covered with a septum and stirred overnight. By the end of the reaction period (15 hours), the reaction mixture had turned from a pale yellow suspension to a solid dark green suspension. Heat was applied to the RBF until the reaction mixture became fluid. The dark green mixture was then added to 1 L of distilled water and ice, and copious precipitation occurred immediately. The precipitate was isolated by vacuum filtration. The precipitate was recrystallized from hot ethanol (1 L). To increase the product yield, the solution was left to stand at room temperature overnight. The crystals were vacuum filtered and the crystals air-dried yielding 58.5 g or 96.7%. The NMR characterization data for the derivative is as follows. 1H NMR (300 MHz, CDCl3): 0.87 (t, J=6.6, 6H, CH2CH3), 1.15-1.6 (m, 28H, CH2(CH2)6), 1.76 (p, J=8.0, 8H, OCH2CH2), 3.89 (s, 3H, OCH3), 3.95 (t, J=6.6, 4H, OCH2CH2), 6.62 (t, J=2.5, 1H, ArH), 7.15 (d, J=2.5, 2H, ArH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07332529B2
Source datasetuspto-grants-2008_02
ORD IDord-c5404a0b178f43f1843248f06cdbb96c
Source noteuspto-grants-2008_02