HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl chloride → 2,6-Di(propan-2-yl)-N-(prop-2-en-1-yl)aniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl chloride | HCID 7850 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Diisopropylaniline | HCID 32484 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2,6-Di(propan-2-yl)-N-(prop-2-en-1-yl)aniline | HCID 71359571 | 84.3% |
Reaction Steps
A solution containing 2,6-diisopropyl aniline (35.4 g, 0.2 mol) and allyl chloride (7.6 g, 0.10 mol) was refluxed for 12 hr and then poured into water (400 ml). Adding an aqueous NaOH solution to the reaction mixture made the mixture basic. After extraction with diethyl ether (3×50 ml) and distillation (73.25 Pa, 92° C.), 18.33 g (84.3%) of N-allyl-2,6-diisopropyl aniline was isolated. Nd30=1.5205. 1H-NMR (ppm,CDCl3): δ=7.10(d, 2H, Ph-Hm), 6.81(t, 1H, Ph-Hp), 6.05(m, 1H, CH═C), 5.34(d, 1H, C═C—Htrans), 5.16(d, 1H, C═C—Hcis), 3.71(broad, 1H, NH), 3.50(d, 2H, CH2—C═C), 3.26(m, 2H, CH(Me)2), 1.28(d, 12H, C═C(CH3)2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07319083B2 |
| Source dataset | uspto-grants-2008_01 |
| ORD ID | ord-9c62d49983df43f1b0c17e32ec0081be |
| Source note | uspto-grants-2008_01 |