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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1846813Generated: October 30, 2026

N-(2-aminophenyl)-3-(benzyloxy)cyclobutanecarboxamide → 2-(3-(Benzyloxy)cyclobutyl)-1H-benzo[d]imidazole

https://huagongshe.com/reaction/1846813

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(2-aminophenyl)-3-(benzyloxy)cyclobutanecarboxamideHCID 67478928—
SolventAcetic AcidHCID 176—
Product2-(3-(Benzyloxy)cyclobutyl)-1H-benzo[d]imidazoleHCID 67481374—

Reaction Steps

A solution of N-(2-aminophenyl)-3-(benzyloxy)cyclobutanecarboxamide (1.78 g, 6.01 mmol) in acetic acid was heated to 100° C. for 1 h, then cooled to RT. The acetic acid was removed in vacuo and ethyl acetate was added to the resulting oil. The resulting suspension was filtered and the collected solid was air dried to give 2-(3-(Benzyloxy)cyclobutyl)-1H-benzo[d]imidazole. The filtrate was concentrated in vacuo to give another suspension, which was filtered, air dried, and added to the first crop of product to give a total of 0.96 g (3.43 mmol, 57% yield) of 2-(3-(Benzyloxy)cyclobutyl)-1H-benzo[d]imidazole as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952037B2
Source datasetuspto-grants-2015_02
ORD IDord-bf13e5d5f2164d6cb61b3aef6506404a
Source noteuspto-grants-2015_02