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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1094724Generated: November 2, 2026

Acetaldehyde → N-ethyl-N-(trifluoroethyl)amine hydrochloride

https://huagongshe.com/reaction/1094724

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetaldehydeHCID 177—
ReactantTriethylamineHCID 8471—
Reactant2,2,2-Trifluoroethylamine hydrochlorideHCID 9772—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
ProductN-ethyl-N-(trifluoroethyl)amine hydrochlorideHCID 42919629743.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2,2,2-trifluoroethylamine hydrochloride (0.5 g, 3.7 mmol) in MeOH (5 mL) was added triethylamine (0.51 mL, 0.37 mmol) followed by acetaldehyde (1.0 mL, excess). The reaction mixture was then stirred at 0° C. for 3 h. Sodium borohydride (1 g, 5.9 mmol) was then added and the reaction mixture was stirred at 0° C. for 20 min. The reaction was quenched with 1M NaOH (10 mL) and the aqueous layer was extracted with DCM (25 mL). The organic layer was separated and to it was added 2M HCl in Et2O (10 mL). The resultant precipitate was filtered to give 0.45 g of N-ethyl-2,2,2-trifluoroethanamine hydrochloride, (yield: 75%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08133998B2
Source datasetuspto-grants-2012_03
ORD IDord-57653ee4763c4c8dadf7e43c8a6e9a1d
Source noteuspto-grants-2012_03