HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1899771Generated: November 1, 2026
Propionitrile → 1-Ethyl-1-(2-propenyl)-3-butenylamine
https://huagongshe.com/reaction/1899771
Participants
| Role | Name | HCID | Charge |
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| Reactant | Propionitrile | HCID 7854 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 22102258 | HCID 22102258 | — |
| Reactant | HCID 178455853 | HCID 178455853 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-Ethyl-1-(2-propenyl)-3-butenylamine | HCID 49962099 | 34% |
Reaction Steps
1-Ethyl-1-(2-propenyl)-3-butenyl isocyanate: A solution of propionitrile (14.5 g, 264 mmol) in dry Et2O (40 mL) was added dropwise to 1.0M allyl magnesium bromide/Et2O (880 mL). The reaction mixture was mechanically stirred at reflux for 2 h, after which time it was cooled to 0°. A saturated aqueous solution of NH4Cl (320 mL) was added cautiously to the cooled reaction mixture. The organic phase was separated, dried (MgSO4), cooled to 0° and then mixed at the same temperature with 1M HCl/Et2O (200 mL). The resulting solid was collected and dried under reduced pressure (ca 27 g). The latter material dissolved in CH2Cl2 (200 mL). The solution was washed with a 10% (w/v) aqueous solution of Na2CO3 (2×) and then brine, dried (MgSO4) and concentrated to dryness to afford a yellow oil. The oil was distilled (82°-85°/20 Torr) to give 1-ethyl-1-(2-propenyl)-3-butenylamine as a colorless liquid (11.6 g, 34%); 1H NMR(CDCl3), 400 MHz) δ 0.89 (t, J=7 Hz, 3H), 1.39 (q, J=7 Hz, 2H), 2.11 (d, J=7 Hz, 2H), 5.06-5.14 (m, 4H), 5.80-5.89 (m, 2H ).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05574015 |
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| Source dataset | uspto-grants-1996_11 |
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| ORD ID | ord-3a50c2c8dadb4325a3913241ee1ca78b |
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| Source note | uspto-grants-1996_11 |
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