HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 337632Generated: October 26, 2026
Sulfuric acid magnesium salt (1:1) → N-[(3,5-dibromophenyl)methyl]cyclopropanamine
https://huagongshe.com/reaction/337632
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric acid magnesium salt (1:1) | HCID 24083 | — |
| Reactant | Cyclopropylamine | HCID 69828 | — |
| Reactant | 3,5-Dibromobenzaldehyde | HCID 622077 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-[(3,5-dibromophenyl)methyl]cyclopropanamine | HCID 67062206 | — |
Reaction Steps
3,5-Dibromobenzaldehyde (1 eq.), cyclopropylamine (2 eq.) and magnesium sulfate (1 eq.) were stirred in dichloromethane (0.1 M) for 20 h. The insolubles were then removed via filtration through a pad of celite and washed further with dichloromethane. The filtrate was concentrated in vacuo to afford the crude imine which was then immediately re-taken up in MeOH (0.1 M). To this solution was added sodium borohydride (5 eq.) portionwise and the resulting mixture was stirred at RT for 4 h. The reaction was quenched with 1 N aq. HCl, neutralized with 1 N aq. NaOH and extracted with ether. The combined organic extracts were then washed further with water and brine, dried over MgSO4, and filtered. Concentration of the filtrate in vacuo afforded the title compound as a pale yellow oil.
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-beae98180f364a6ea6f2518568cf3d56 |
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| Source note | uspto-grants-2014_11 |
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