HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1725219Generated: October 25, 2026
Borane → Benzenemethanamine, N-ethyl-4-(trifluoromethoxy)-
https://huagongshe.com/reaction/1725219
Participants
| Role | Name | HCID | Charge |
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| Reactant | Borane | HCID 6331 | — |
| Reactant | N-{[4-(Trifluoromethoxy)phenyl]methyl}acetamide | HCID 44542707 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Benzenemethanamine, N-ethyl-4-(trifluoromethoxy)- | HCID 20117720 | 21% |
Reaction Steps
N-[4-(Trifluoromethoxy)benzyl]acetamide (10.4 g, 44.6 mmol) was dissolved in THF (100 mL) and cooled to −10° C. Borane (56 mL of a 2 M solution of the dimethylsulfide complex in diethyl ether) was added and the reaction mixture was stirrred at −10° C. for 15 minuters and was then allowed to warm to room temperature. The reaction mixture was refluxed overnight and was then allowed to cool to room temperature. The reaction was quenched by careful addition of 10% HCl (30 mL) at 0° C. and the mixture was stirred at room temperature overnight and then concentrated in vacuo. The residue was taken up in water (200 mL) and diethyl ether (200 mL) and the phases were separated. Concentration in vacuo of the diethyl ether phase afforded 1.9 g (21%) of the title compound as a colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07488844B2 |
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| Source dataset | uspto-grants-2009_02 |
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| ORD ID | ord-f480508e59f9442c99ffad836b92edc7 |
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| Source note | uspto-grants-2009_02 |
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