HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 337643Generated: October 28, 2026
Sulfuric acid magnesium salt (1:1) → N-[3-[(1E)-3-Methoxyprop-1-en-1-yl]-5-(trifluoromethyl)benzyl]cyclopropanamine
https://huagongshe.com/reaction/337643
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuric acid magnesium salt (1:1) | HCID 24083 | — |
| Reactant | Cyclopropylamine | HCID 69828 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 3-[(1E)-3-Methoxyprop-1-en-1-yl]-5-(trifluoromethyl)benzaldehyde | HCID 86651682 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-[3-[(1E)-3-Methoxyprop-1-en-1-yl]-5-(trifluoromethyl)benzyl]cyclopropanamine | HCID 67062106 | — |
Reaction Steps
3-[(1E)-3-Methoxyprop-1-en-1-yl]-5-(trifluoromethyl)benzaldehyde (1 eq.) from the previous step and cyclopropylamine (2 eq.) were combined in CH2Cl2 (0.2 M). To this was then added MgSO4 (1.5 eq.) and the resulting suspension was stirred at RT for 18 h. The insolubles were then removed via filtration through a pad of celite and the filtrate was concentrated in vacuo. The crude imine thus obtained was then re-taken up in a 2:1 (v/v) mixture of THF:MeOH (0.2 M). To this solution was added sodium borohydride (5 eq.) portionwise and the resulting mixture was stirred at RT for 18 h. The reaction was quenched with saturated aqueous sodium bicarbonate and extracted with ethyl acetate. The combined organic extracts were then washed with brine, dried over Na2SO4, filtered and the filtrate concentrated in vacuo. Purification of the crude product by way of flash chromatography (SiO2, 9:1 (v/v) Hex:EtOAc→EtOAc) afforded the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08889714B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-092aa81d5a854ccea7e5b152928344f0 |
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| Source note | uspto-grants-2014_11 |
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