HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanolamine → 2-Cycloheptylamino-ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | Bromocycloheptane | HCID 16992 | — |
| Product | 2-Cycloheptylamino-ethanol | HCID 12217891 | — |
Reaction Steps
2-Hydroxyethylamine was reacted with cycloheptyl bromide according to Method B2a to give N-cycloheptyl-N-(2-hydroxyethyl)amine. The alcohol was reacted with SOCl2 according to Method B7c to give N-cycloheptyl-N-(2-chloroethyl)ammonium chloride. The chloroethylamine was reacted with 2-methyl-4-nitrophenyl isothiocyanate to give 2-(2-methyl-4-nitrophenylimino)-3-cycloheptyl-1,3-thiazolidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06353006B1 |
| Source dataset | uspto-grants-2002_03 |
| ORD ID | ord-f63e4eabee7f4de98724ce9d245b45f2 |
| Source note | uspto-grants-2002_03 |