HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isopropanol → Dipropan-2-yl(4-nitrophenyl)phosphonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | (4-Nitrophenyl)phosphonic dichloride | HCID 13486298 | — |
| Product | Dipropan-2-yl(4-nitrophenyl)phosphonate | HCID 11572803 | 25% |
Reaction Steps
A solution of distilled dry propan-2-ol (20 ml) and triethylamine (1.0 g, 10 mmol) was added dropwise to (4-nitrophenyl)phosphonic dichloride (1.2 g, 5 mmol) at 0° C. The resulting mixture was stirred at reflux overnight, the mixture filtered and the filtrate concentrated under reduced pressure to yield a crude product, which was purified by chromatography over silica gel eluting with petroleum ether:EtOAc: 5:1 to afford 360 mg of desired dipropan-2-yl (4-nitrophenyl)phosphonate (yield: 25%). 1H-NMR (CDCl3, 400 MHz): δ=1.18 (d, J=6.0 Hz, 6 H), 1.33 (d, J=6.4 Hz, 6 H), 4.65-4.73 (m, 2 H), 7.93 (dd, J=8.8, 12.8 Hz, 2 H), 8.22 (dd, J=3.2, 8.8 Hz, 2 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09096624B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-d09f6be7053345c586193bc1e745b82a |
| Source note | uspto-grants-2015_08 |