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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetaldehyde | HCID 177 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2,2,2-Trifluoroethylamine hydrochloride | HCID 9772 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-ethyl-N-(trifluoroethyl)amine hydrochloride | HCID 42919629 | 743.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08133998B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-57653ee4763c4c8dadf7e43c8a6e9a1d |
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| Source note | uspto-grants-2012_03 |
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