HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acrylonitrile → N-(2-cyanoethyl)-N',N'-dimethyl-1,4-diaminobutane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acrylonitrile | HCID 7855 | — |
| Reactant | 4-Dimethylaminobutylamine | HCID 77063 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-(2-cyanoethyl)-N',N'-dimethyl-1,4-diaminobutane | HCID 18934680 | 80% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
A solution of acrylonitrile (1.17 g, 22.07 mmol) in methanol (1.0 ml) was added dropwise to a solution of N,N-dimethyl-1,4-diaminobutane 322 (2.1 g, 18.42 mmol) in methanol (1.0 ml) at 0° C., and the mixture was stirred at 0° C. for sixteen hours. Evaporation of the solvent in vacuo afforded almost pure N-(2-cyanoethyl)-N',N'-dimethyl-1,4-diaminobutane 323 as a colorless oil (2.5 g, 80% yield based on 322). 1H NMR (400 MHz, CDCl3) δ: 1.45 (4H, m, --CH2 --CH2 --CH2 --CH2 --), 2.15 (6H, s, --N(CH3)2), 2.22 (2H, t, --CH2N), 2.47 (2H, t, --CH2CH2CN), 2.60 (2H, t, --CH2CH2NH--), 2.88 (2H, t, --CH2CH2NH--), 3.37 (1H, s, --NH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05733899 |
| Source dataset | uspto-grants-1998_03 |
| ORD ID | ord-84edcdeb710843f298afe85eff4bc91e |
| Source note | uspto-grants-1998_03 |