HuagongsheHuagongshe Chemistry Print Report · For research reference only
Epichlorohydrin → N-Butyl-N-[(oxiran-2-yl)methyl]butan-1-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Epichlorohydrin | HCID 7835 | — |
| Reactant | Dibutylamine | HCID 8148 | — |
| Product | N-Butyl-N-[(oxiran-2-yl)methyl]butan-1-amine | HCID 12401886 | 20.2% |
Reaction Steps
A stirred solution of epichlorohydrin (20.0 g, 0.22 mole) is treated dropwise with di-n-butylamine (29.73 g, 0.23 mole) over a 1 hour period followed by continued stirring at room temperature overnight. The reaction mixture is washed with 20% K2CO3 (50 ml). The organic layer is then stirred with 40% NaOH for 1 hour and then extracted with 3×100 ml portions of ether. The etheral extracts are pooled and washed with H2O (100 ml). The organic layer is dried over anhydrous Na2SO4 and filtered. The filtrate is concentrated under reduced pressure to leave the crude product (I) weighing 39.42 g. The crude product is distilled at 52°/0.15 mmHg to give 8.24 g (20.2%) pure product to be used as an intermediate in Part B.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05922703 |
| Source dataset | uspto-grants-1999_07 |
| ORD ID | ord-0c9cc6dfee794036b6db7416bb43a02b |
| Source note | uspto-grants-1999_07 |