Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tert-Butylamine | HCID 6385 | — |
| Reactant | Cyclohexene oxide | HCID 9246 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 11695501 | HCID 11695501 | 92.4% |
Reaction Steps
A mixture of cyclohexene oxide (19.6 g), t-butyl amine (37.1 g), zinc chloride (2.5 g), and 50 ml of toluene were sealed under an inert atmosphere in a Diels-Alder flask. The contents were stirred and heated in a sand bath at 120° C. for 23 hours. After cooling the slurry was diluted with 100 ml of toluene, washed with dilute ammonium hydroxide solution (3×250 ml) and water (300 ml), dried (Na2SO4), filtered, and the solvents were removed under reduced pressure to give 31.6 g of N-2-hydroxycyclohexyl-N-t-butylamine as an off-white, waxy solid, m.p. 42°-44° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04624980 |
|---|
| Source dataset | uspto-grants-1986_11 |
|---|
| ORD ID | ord-99fbf91923e040d7b8abdf67cd57d023 |
|---|
| Source note | uspto-grants-1986_11 |
|---|