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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1658261Generated: October 26, 2026

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

https://huagongshe.com/reaction/1658261

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Nitroamino-2-imidazolineHCID 410042—
Reactant2-Amino-1-(3-chlorophenyl)ethan-1-olHCID 3751601—
SolventO-XyleneHCID 7237—
Productm-Chloro-alpha-(2-imidazolin-2-ylaminomethyl)benzyl alcoholHCID 54186887—

Reaction Steps

A mixture of 9.5 parts of α-(aminomethyl)-m-chlorobenzyl alcohol, 7.15 parts of 2-(nitramino)-2-imidazoline and 40 parts of xylene is stirred in an oil-bath at 150°-160°C. while a great part of the xylene is distilled off. The resulting residue is diluted with a few parts of acetone and the product is allowed to crystallize. It is filtered off and crystallized from 4-methyl-2-pentanone, yielding m-chloro-α-(2-imidazolin-2-ylaminomethyl)benzyl alcohol; m.p. 108.5°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03963718
Source datasetuspto-grants-1976_06
ORD IDord-ce9d67d15e564b8a86802fa48941c75a
Source noteuspto-grants-1976_06