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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 480967Generated: October 25, 2026

Diisopropylethylamine → N-(4-cyanobenzyl)-4-formylbenzamide

https://huagongshe.com/reaction/480967

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant4-(Aminomethyl)benzonitrileHCID 82608—
Reactant4-Formylbenzoyl chlorideHCID 12424620—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
ProductN-(4-cyanobenzyl)-4-formylbenzamideHCID 1876629655.5%

Reaction Steps

In the same manner as that described in Example 2(1), a reaction was carried out using 4-cyanobenzylamine (329 mg, 2.5 mmol), described in J. Am. Chem. Soc., 81, 4328 (1959), N,N-diisopropylethylamine (0.91 ml, 5.2 mmol), 4-formylbenzoyl chloride (350 mg, 2.1 mmol) and 4-(dimethylamino)pyridine (a catalytic amount) and the reaction mixture was treated according to a similar procedure to that described in Example 2(1) to afford N-(4-cyanobenzyl)-4-formylbenzamide (308 mg, yield 56) as a white solid which was recrystallized from ethyl acetate to give white fluffy crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06653330B2
Source datasetuspto-grants-2003_11
ORD IDord-28a3923c3b2e4f219bf0ea0f308da85c
Source noteuspto-grants-2003_11