HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbodiimide → N-[3-(dimethyl-amino)]propyl-N'-(3-morpholino)propyl-carbodiimide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbodiimide | HCID 160435 | — |
| Reactant | N-[3-(dimethylamino)]propyl-N'-(3-morpholino)propyl-thiourea | HCID 54184092 | — |
| Catalyst | Mercuric oxide | HCID 30856 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | N-[3-(dimethyl-amino)]propyl-N'-(3-morpholino)propyl-carbodiimide | HCID 10923093 | 60% |
Reaction Steps
In 35 ml of acetone was dissolved 2.7 g (10 mmol) of N-[3-(dimethylamino)]propyl-N'-(3-morpholino)propyl -thiourea (Compound (1)). Further, 4.2 g (20 mmol) of mercury oxide was added, and the resulting mixture was stirred for 2 hours under reflux. Then, the reaction mixture was allowed to cool and filtered. The solvent was distilled off to obtain a crude product. This product was evaporated under reduced pressure to obtain 1.5 g (yield: 60%) of N-[3-(dimethyl-amino)]propyl-N'-(3-morpholino)propyl-carbodiimide (Compound (2) in the following reaction formula (1)). Its boiling point (b.p.) was from 125° to 128° C./0.2 mmHg. NMR spectrum data of Compound (2) are shown below.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05856479 |
| Source dataset | uspto-grants-1999_01 |
| ORD ID | ord-b049bfa0a79e480e9607b1981e115b55 |
| Source note | uspto-grants-1999_01 |