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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1903179Generated: November 3, 2026

4-Methoxybenzaldehyde → 3-Butyl-2-(4-methoxyphenyl)-3H-naphtho[1,2-d]imidazole

https://huagongshe.com/reaction/1903179

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethoxybenzaldehydeHCID 31244—
ReactantHCID 20468286HCID 20468286—
Product3-Butyl-2-(4-methoxyphenyl)-3H-naphtho[1,2-d]imidazoleHCID 1327442053%

Reaction Steps

The compound of the title is prepared by following essentially the same procedure described in example 2 but starting from 2-butylamino-1-nitrosonaphthalene instead of 2-methylamino-1-nitrosonaphthalene and employing 4-methoxybenzaldehyde instead of 4-ethoxybenzaldehyde. Yield 53%. M.p. 99,5°-100,5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04435417
Source datasetuspto-grants-1984_03
ORD IDord-79a8375b633541269f4032120f06fd0c
Source noteuspto-grants-1984_03