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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1576845Generated: October 24, 2026

2-Nitroamino-2-imidazoline → p-Chloro-alpha-(2-imidazolin-2-ylaminomethyl)benzyl alcohol

https://huagongshe.com/en/reaction/1576845

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Nitroamino-2-imidazolineHCID 410042—
Reactant2-Amino-1-(4-chlorophenyl)ethan-1-olHCID 412434—
SolventO-XyleneHCID 7237—
Productp-Chloro-alpha-(2-imidazolin-2-ylaminomethyl)benzyl alcoholHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03983133
Source datasetuspto-grants-1976_09
ORD IDord-639571b03b6a485b96f77ebac7b9a34e
Source noteuspto-grants-1976_09