HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 654566Generated: October 30, 2026
Dichloromethane → Piperidine, 1,1'-carbonyldi-
https://huagongshe.com/reaction/654566
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Phosgene | HCID 6371 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Water | HCID 962 | — |
| Product | Piperidine, 1,1'-carbonyldi- | HCID 21493 | 96% |
Reaction Steps
Phosgene was passed for 17 minutes, at the rate of 3 grams per minute, through a mixture of 84 grams (1 mole) of piperidine, 500 ml. of methylene chloride and 100 ml. of water. The pH was maintained in the range of 8-11 by the addition of 50% aqueous sodium hydroxide solution during the latter portion of the phosgene passage. An exothermic reaction occurred which caused refluxing of the mixture. After phosgenation was complete, additional base was added until the pH remained constant at 11 for 5 minutes, after which 200 ml. of water was added and the organic layer was removed, washed twice with aqueous hydrochloric acid solution and filtered. Upon vacuum stripping, the desired bis(pentamethylene)urea was obtained in 96% yield. Its structure was confirmed by proton nuclear magnetic resonance spectroscopy.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05132423 |
|---|
| Source dataset | uspto-grants-1992_07 |
|---|
| ORD ID | ord-d965484c2b3f4372847bff05bef2ec79 |
|---|
| Source note | uspto-grants-1992_07 |
|---|