HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hexamethylenediamine → Butyl ethyl-3-hydroxypropylphosphinate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hexamethylenediamine | HCID 16402 | — |
| Reactant | Butyl ethyl(2-formylethyl)phosphinate | HCID 86656679 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Nickel | HCID 935 | — |
| Catalyst | Potassium Hydroxide | HCID 14797 | — |
| Solvent | Water | HCID 962 | — |
| Product | Butyl ethyl-3-hydroxypropylphosphinate | HCID 86656676 | 83% |
Reaction Steps
In a glass autoclave, 240 g of hexamethylenediamine, 52 g of water, 6.4 g of Raney® nickel (doped with 1.5% by weight of chromium), 0.18 g (4 mmol) of potassium hydroxide, 75.1 g (0.37 mol) of butyl ethyl(2-formylethyl)phosphinate (produced in as Example 9) are reacted at 50° C. with hydrogen at 25 bar. Following a reaction time of 8 hours, the autoclave was let down. For purification, the reaction solution is filtered, passed through a column charged with Deloxan® THP II and concentrated in vacuo. The product is purified by chromatography to obtain 63.9 g (83% of theory) of butyl ethyl(3-hydroxypropyl)phosphinate as colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08604108B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-0380eebd071740d2bd2dca1f029adfcf |
| Source note | uspto-grants-2013_12 |