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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1436908Generated: November 1, 2026

Ethylamine → N-(3,5-bistrifluoromethylbenzyl)-N-ethylamine

https://huagongshe.com/reaction/1436908

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylamineHCID 6341—
ReactantTetrahydrofuranHCID 8028—
Reactant3,5-Bis(trifluoromethyl)benzaldehydeHCID 136247—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
ProductN-(3,5-bistrifluoromethylbenzyl)-N-ethylamineHCID 59735055—

Reaction Steps

In 20 ml of methanol was dissolved 24.5 g of 3,5-bistrifluoromethylbenzaldehyde, and under ice-cooling, added thereto was 60 ml of ethylamine (a 2M tetrahydrofuran solution). Subsequently, 4.38 g of sodium borohydride was slowly added thereto, and the mixture was stirred at room temperature for 3 hours. To the reaction mixture was added distilled water and concentrated under reduced pressure. The residue was extracted with dichloromethane, and the organic layer was dried and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=4:1→chloroform:methanol=9:1), to give 6.35 g of N-(3,5-bistrifluoromethylbenzyl)-N-ethylamine as shown in Table 135 below.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07619092B2
Source datasetuspto-grants-2009_11
ORD IDord-2dc5eb58397d403f947fcb526c49a766
Source noteuspto-grants-2009_11