HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethyl 2,2',2''-(1,4,7,10-tetraazacyclododecane-1,4,7-triyl)triacetate → HCID 67600976, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethyl 2,2',2''-(1,4,7,10-tetraazacyclododecane-1,4,7-triyl)triacetate | HCID 10906130 | — |
| Reactant | HCID 86754142 | HCID 86754142 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 67600976 | HCID 67600976 | — |
Reaction Steps
200 ml of absolute ethanol is poured over 8.61 g (20 mmol) of N,N',N"-tris-(ethoxycarbonylmethyl)-1,4,7,10-tetraazacyclododecane (produced according to DE 36 25 417 A1) in a bomb tube. After 4.15 g (20 mmol) of N-butyl-N-[(2-oxiranyl)-methyl]-methanesulfonic acid amide is added (Example 2a), the bomb tube is closed, flushed with nitrogen, and the resulting reaction mixture is heated for 16 hours to 90° C. After the reaction (TLC control) is completed, the solvent is evaporated in a vacuum and the yellowish, oily residue is chromatographed on silica gel (eluent: chloroform/methanol; methanol: 0-80%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05919431 |
| Source dataset | uspto-grants-1999_07 |
| ORD ID | ord-ede51fa60aa3499785d09c062c1c6929 |
| Source note | uspto-grants-1999_07 |