HuagongsheHuagongshe Chemistry Print Report · For research reference only
Epichlorohydrin → n-[1-(4-Chlorophenyl)-1-methylethyl]-2,3-epoxypropylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Epichlorohydrin | HCID 7835 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-(4-Chlorophenyl)-1-methylethylamine | HCID 11030256 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | n-[1-(4-Chlorophenyl)-1-methylethyl]-2,3-epoxypropylamine | HCID 18349585 | — |
Reaction Steps
Epichlorohydrin (8.05 ml) was added dropwise to a solution of 1-(4-chlorophenyl)-1-methylethylamine (17.38 g) in methanol (17.5 ml) at 0° C. with stirring. The solution was warmed to ambient temperature and stirred for 48 hours. Sodium hydroxide solution (50%) (17.5 ml) was added and the mixture stirred for 15 minutes. The product was extracted with ether to give an oil which was purified by flash column chromatography on silica using petroleum ether, b.p. 40-60° C./ethyl acetate/triethylamine (8:2:1) as the mobile phase with gradually increasing amounts of ethyl acetate to give N-[1-(4-chlorophenyl)-1-methylethyl]-2,3-epoxypropylamine as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06215001B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-8d010dca0ef24c079fbc3cbfa2152aba |
| Source note | uspto-grants-2001_04 |