HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Ethanediamine, N1,N1,N2-trimethyl- → Bis-benzyloxy benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Ethanediamine, N1,N1,N2-trimethyl- | HCID 67338 | — |
| Reactant | Methyl 2,3-bis(benzyloxy)benzoate | HCID 10665397 | — |
| Product | Bis-benzyloxy benzoic acid | HCID 10520703 | — |
Reaction Steps
In another embodiment the compounds can be prepared as shown in Scheme IV. A bromo-nitrobenzene (1) can be reacted with N1, N2, N2 trimethylethane-1,2-diamine to give N1-(nitrophenyl)-N1, N2, N2-trimethylethane-1,2-diamine (2). A solution of (2) in can be subjected to hydrogenation, passed through a short pad of celite, washed with MeOH and evaporated under reduced pressure. Thiocarbodiimidazole can then be added to (2) to give the N1-(isothiocyanato-phenyl)-)-N1, N2, N2-trimethylethane-1,2-diamine (3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08742133B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-ad0cb0e7488b42dfae8553e39ba4c714 |
| Source note | uspto-grants-2014_06 |