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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2380799Generated: October 31, 2026

Hydrochloric Acid → Methyl 4-[(dimethylamino)diazenyl]thiophene-2-carboxylate

https://huagongshe.com/reaction/2380799

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDimethylamineHCID 674—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 4-aminothiophene-2-carboxylateHCID 10773224—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
ProductMethyl 4-[(dimethylamino)diazenyl]thiophene-2-carboxylateHCID 6718371710.8%

Reaction Conditions

Temperature2.5 °C

Reaction Steps

To a solution of methyl 4-aminothiophene-2-carboxylate (1.7 g, 10.82 mmol) and cone. HCl (4.6 mL, 43.5 mmol) in H2O (20 mL) was added NaNO2 (0.84 g, 12.17 mmol) in portions for 5 min at 0° C. After stirring for 0.5 h at 0-5° C., the reaction mixture was added to the solution of K2CO3 (5.8 g, 42 mmol) and dimethylamine (4.6 mL, 40%, 40.9 mmol) in H2O (30 mL) at 0° C. The mixture was stirred at 0-5° C. for 1 h and poured into ice cold water. The solution was extracted with chloroform (3×100 mL). The combined CHCl3 layer was washed with water, brine and dried over sodium sulfate. The solution was filtered and evaporated the solvent. The residue was chromatographed over silica gel column using hexane-EtOAc (80:20) as eluents to give the product as light red color solid (250 mg), which was recrystallized from chloroform-hexane (110 mg), mp 90-92° C. 1H NMR (400 MHz, CDCl3): δ 7.93 (1H, d, J=1.6 Hz), 7.31 (1H, d, J=1.6 Hz), 3.88 (3H, s), 3.31 (6H, br s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08258119B2
Source datasetuspto-grants-2012_09
ORD IDord-bf1c337be5db4f2494f51162280453f0
Source noteuspto-grants-2012_09