HuagongsheHuagongshe Chemistry Print Report · For research reference only
Glycerol → tert-Butylisobutyl-n-propylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Glycerol | HCID 753 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1-Iodopropane | HCID 33643 | — |
| Reactant | N-tert-butyl-2-methylpropan-1-amine | HCID 527145 | — |
| Product | tert-Butylisobutyl-n-propylamine | HCID 21195175 | — |
Reaction Steps
A mixture of tert-butylisobutylamine (19.39 g, 0.15 mol), 1-iodopropane (20.40 g, 0.12 mol) and glycerol (5.53 g, 60 mmol) was refluxed for 40 h. Aqueous 8 M potassium hydroxide (30 ml, 0.24 mol) was added, the organic layer was separated and the aqueous layer was extracted with n-pentane (50 ml). The organic solutions were combined, dried over anhydrous magnesium sulfate and the product was isolated by distillation to yield 12.52 g, (61%), bp 72-73° C./18 mm Hg; 1H NMR (CDCl3) δ0.80 (t, J=6.2 Hz, 3H, CH3), 0.84 (d, J=6.6 Hz, 6H, CH3), 1.01 (s, 9H, CH3), 1.40 (sextet, J=6.2 Hz, 2H, CH2), 159 (nonet, J=6.6 Hz, 1H, CH), 2.16 (d, J=6.6 Hz, 2H, CH2), 2.34 (m, 2H, CH2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06248885B1 |
| Source dataset | uspto-grants-2001_06 |
| ORD ID | ord-6a56ebd3eca14a26aa771b6ccc426d0c |
| Source note | uspto-grants-2001_06 |