Solvent-free method for preparing sterically hindered phosphoramidates
US6277988A · kind A · utility
Assignee
Inventors
Key dates
| Filing date | Feb 29, 2000 |
| Grant date | Aug 21, 2001 |
| Priority date | — |
| Expiry date | Feb 29, 2020 |
Classification
- Technology area (CPC C)Chemistry; Metallurgy
- CPC primaryC07F9/6521
- WIPO fieldOrganic fine chemistry
- WIPO sectorChemistry
Abstract
Sterically hindered phosphoramidates such as N,N'-bis[di-(2,6-xylenoxy)phosphinyl]piperazine are prepared by the reaction of a sterically hindered diaryl chlorophosphate, such as di-(2,6-xylyl) chlorophosphate, with a basic nitrogen compound containing at least two basic N--H groups, preferably a heterocyclic compound such as piperazine, in a predominantly liquid, solvent-free reaction mixture. The reaction may be conducted in the melt or in the presence of a non-solvent carrier, typically an aliphatic hydrocarbon. An excess of the basic nitrogen compound is employed as an acid acceptor.
Source: USPTO / EPO open patent data. Objective bibliographic and citation counts.