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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1072510Generated: November 3, 2026

2,4-Dichlorobenzaldehyde → Cyclopropyl-(2,4-dichloro-benzyl)-amine

https://huagongshe.com/reaction/1072510

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-DichlorobenzaldehydeHCID 13404—
ReactantCyclopropylamineHCID 69828—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
ProductCyclopropyl-(2,4-dichloro-benzyl)-amineHCID 4720306—

Reaction Steps

5.25 g (30 mmol) of 2,4-dichlorobenzaldehyde was introduced into 140 ml of methanol and, at room temperature, a solution of 1.71 g (30 mmol) of cyclopropylamine was added. The mixture as stirred at room temperature for 40 min and then 1.42 g (37.5 mmol) of NaBH4 was added in portions. After standing overnight, the solvent was removed and the residue was taken up in 2 N HCl. Two extractions with ethyl acetate were carried out. The aqueous phase was made alkaline with NaOH and again extracted twice with ethyl acetate. The organic phases were dried with MgSO4 and concentrated. The crude product obtained in this way, in the form of a slightly yellowish oil, was reacted further without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06911453B2
Source datasetuspto-grants-2005_06
ORD IDord-a8393593614e4b228a41f526143ec7c0
Source noteuspto-grants-2005_06