HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium formate → N4,N7,N10-Triscarboxymethyl-1,13-bishydroxy-5,9-bishydroxymethyl-4,7,10-triazatridecane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | N4, N7, N10-Triscarboxymethyl-1,13-bisbenzyloxy-5,9-bisbenzyloxymethyl-4,7,10-triazatridecane | HCID 86746667 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N4,N7,N10-Triscarboxymethyl-1,13-bishydroxy-5,9-bishydroxymethyl-4,7,10-triazatridecane | HCID 86748685 | — |
Reaction Steps
N4,N7,N10 -Triscarboxymethyl-1,13-bisbenzyloxy-5,9-bisbenzyloxymethyl-4,7,10-triazatridecane (0.30 g, 0.4 mmol) was dissolved in methanol (15 ml), 10% Palladium on carbon (0.3 g) and ammonium formate (0.1 g) were added and the mixture was kept at 50° C. for 16 hours. The catalyst was filtered off and washed with methanol (5 ml). The filtrate was evaporated and the title compound was isolated as a white powder. Yield 0.14 g (95%). M.p. 173°-177° C. The structure was confirmed by 1H NMR and 13CNMR.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05531978 |
| Source dataset | uspto-grants-1996_07 |
| ORD ID | ord-5033aa686fdf4f5bbb1b0cacf9411af7 |
| Source note | uspto-grants-1996_07 |