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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1456884Generated: October 30, 2026

Hydrochloric Acid → HCID 15702830, compound

https://huagongshe.com/reaction/1456884

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant1,4,7-Tris(carboxymethyl)-1,4,7,10-tetraazacyclododecaneHCID 107830—
ReactantAceton-methanolHCID 21894497—
SolventMethanolHCID 887—
ProductHCID 15702830HCID 15702830—

Reaction Steps

To a solution of 250 mg (0.723 mmol) of 1,4,7-triscarboxymethyl-1,4,7,10-tetraazacyclododecane in 2.9 ml of methanol was added 220 mg (1.59 mmol) of potassium carbonate. To the resulting mixture was added 308 mg (2.17 mmol, 3 equiv) of methyl iodide. Within a short time, most of the solids dissolved. After 15 hours at 21° C., a mass of crystals had separated. Additional methanol was added (2 ml) to dissolve the solid. After 23 hours, an additional 102 mg (0.72 mmol) of methyl iodide was added. After an additional 16 hours, the solution was acidified with concentrated hydrochloric acid and the volatiles were removed on the rotary evaporator. The residue was extracted with methanol, filtered, and the methanol evaporated. The residue was crystallized twice from methanol/acetone yielding 56 mg (0.16 mmol) of a colorless solid, melting point 215°-240° (dec.). 13C NMR (D2O, ppm vs TMS): 177.2, 171.1, 57.2, 56.5, 54.1, 52.6, 50.1, 49.9, 43.7. Mass spectrum (FAB): m/e 359 (M-H) and 361 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05846519
Source datasetuspto-grants-1998_12
ORD IDord-bddafd4cc1bb46e098c0c94727b7728b
Source noteuspto-grants-1998_12