HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium nitrate → 1,1-Diethoxy-2-butene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium nitrate | HCID 22985 | — |
| Reactant | Ethyl orthoformate | HCID 31214 | — |
| Reactant | Crotonaldehyde | HCID 447466 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1,1-Diethoxy-2-butene | HCID 99778 | 89% |
Reaction Steps
Crotonaldehyde (23.64 mL, 285.35 mmol), triethyl orthoformate (57.02 mL, 342.42 mmol) and ammonium nitrate (2.28 g, 28.54 mmol) were combined in 60 mL EtOH. After 22 h at ambient temperature, the reaction was diluted with EtOAc (60 mL) and washed with saturated sodium bicarbonate solution (40 mL). The aqueous layer was back extracted with EtOAc (20 mL). The combined organics were washed with brine (40 mL), dried over Na2SO4, filtered and concentrated in vacuo to give 36.5 g (89%) of 1,1-diethoxybut-2-ene. 1H NMR (CDCl3, 400 MHz) 5.84 (m, 1H); 5.54 (m, 1H); 4.82 (d, J=5.7 Hz, 1H); 3.64 (m, 2H); 3.49 (m, 2H); 1.73 (m, 3H); 1.21 (m, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08394837B2 |
| Source dataset | uspto-grants-2013_03 |
| ORD ID | ord-0d61e61556834235ad87380cc435a00a |
| Source note | uspto-grants-2013_03 |