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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1097204Generated: November 1, 2026

Hydrochloric Acid → HCID 86646881, compound

https://huagongshe.com/reaction/1097204

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDimethylamineHCID 674—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium NitriteHCID 23668193—
ReactantHCID 86646882HCID 86646882—
SolventWaterHCID 962—
ProductHCID 86646881HCID 8664688143,597.102%

Reaction Conditions

Temperature2.5 °C

Reaction Steps

To a solution of ethyl 3-amino-5-phenylselenophene-2-carboxylate (0.6 g, 2.03 mmol) and conc. HCl (0.79 mL, 8.12 mmol) in water (4.7 mL) was added sodium nitrite (150 mg, 2.23 mmol) in portions for 5 min at 0° C. After stirring at 0-5° C. for 1 h, the reaction mixture was added to the solution of potassium carbonate (1.06 g, 7.7 mmol) and dimethylamine (0.82 mL, 40%, 7.3 mmol) in water (5.7 mL) at 0° C. The mixture was stirred at 0-5° C. for 2 h and poured into ice cold water. The solution was extracted with chloroform (3×100 mL) and the combined 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 (90:10) as eluents to give the product as a dark red color solid (310 g, 44%), mp 82-84° C. 1H NMR (400 MHz, CDCl3): δ 7.80 (1H, s, H-4), 7.58-7.60 (2H, m, Ar—H), 7.31-7.40 (3H, m, Ar—H), 4.33 (2H, q, J=7.0 Hz, —COOCH2—), 3.53 (3H, s, —N—CH3), 3.29 (3H, s, —N—CH3), 1.37 (3H, t, J=7.0 Hz, —COOCH2CH3); LC-MS (positive ion mode): m/z 372, 374 (M+Na)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143237B2
Source datasetuspto-grants-2012_03
ORD IDord-dbdc942002404ee3adc43351b1462abf
Source noteuspto-grants-2012_03