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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1078376Generated: November 1, 2026

4-Chlorobenzaldehyde → 4-(4-Chlorophenyl)butan-1-amine

https://huagongshe.com/reaction/1078376

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ChlorobenzaldehydeHCID 7726—
ReactantSodium borohydrideHCID 4311764—
Reactant1-(3-Aminopropyl)-2-benzyl-4-methylimidazoleHCID 19429356—
SolventEthanolHCID 702—
Product4-(4-Chlorophenyl)butan-1-amineHCID 10773822—

Reaction Steps

In a similar manner to Example 35, a mixture of 4-chlorobenzaldehyde (5.6 g) and 1-(3-aminopropyl)-2-benzyl-4-methylimidazole (9.2 g) in ethanol (100 ml) was stirred and then reduced with sodium borohydride (1.6 g) to give 3-(2-benzyl-4-methylimidazol-1-yl)-[-(4-chlorobenzyl)propylamine, b.p. 190°-200° C. (0.04 mmHg). Glc and 1H nmr indicated that the product contained 21% of 3-(2-benzyl-5-methylimidazol-1-yl)-N-(4-chlorobenzyl)propylamine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05547972
Source datasetuspto-grants-1996_08
ORD IDord-db6e93efa3e549cc86c6f1e4e07fd3eb
Source noteuspto-grants-1996_08