HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol, 2-(cyclohexylamino)- → N-(2-chloroethyl)cyclohexanamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol, 2-(cyclohexylamino)- | HCID 17827 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Product | N-(2-chloroethyl)cyclohexanamine | HCID 410533 | — |
Reaction Steps
2-Hydroxyethylamine and cyclohexanone were reacted according to Method B4a, Step 1 to afford 4-aza-1-oxaspiro[4.5]decane. The oxazolidine was reduced according to method B4a, Step 2 to afford N-cyclohexyl-N-(2-hydroxyethyl)amine. The alcohol was reacted with SOCl2 according to Method B7c to afford N-cyclohexyl-N-(2-chloroethyl)amine. The amine was reacted with 2-methoxy-4-nitrophenyl isothiocyanate according to Method C1d to afford 2-(2-methyl-4-nitrophenylimino)-3-cyclohexyl-1,3-thiazolidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06353006B1 |
| Source dataset | uspto-grants-2002_03 |
| ORD ID | ord-4066b0a77d574dd1a4eb42462eeb6029 |
| Source note | uspto-grants-2002_03 |