HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Nitroamino-2-imidazoline → p-Chloro-alpha-(2-imidazolin-2-ylaminomethyl)benzyl alcohol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Nitroamino-2-imidazoline | HCID 410042 | — |
| Reactant | 2-Amino-1-(4-chlorophenyl)ethan-1-ol | HCID 412434 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | p-Chloro-alpha-(2-imidazolin-2-ylaminomethyl)benzyl alcohol | HCID 54043520 | — |
Reaction Steps
To 5.2 parts of 2-(nitramino)-2-imidazoline is added a solution of 7.5 parts of α-(aminomethyl)-p-chlorobenzyl alcohol in 40 parts of xylene while heating. Upon completion, sitrring is continued while heating in an oil-bath at 150°-160°C. and while the xylene is partly distilled off (till gas evolution ceases). The residue is cooled and after the addition of a few parts of acetone, the product is allowed to crystallize. It is filtered off, washed successively with acetone and diisopropylether, dried and the product is recrystallized from 4-methyl-2-pentanone, yielding p-chloro-α-(2-imidazolin-2-ylaminomethyl)benzyl alcohol; m.p. 156°-158°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03983133 |
| Source dataset | uspto-grants-1976_09 |
| ORD ID | ord-639571b03b6a485b96f77ebac7b9a34e |
| Source note | uspto-grants-1976_09 |