HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 931497Generated: October 25, 2026
Dimethylamine → 4-Bromo-N,N-dimethylbenzylamine
https://huagongshe.com/reaction/931497
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Bromobenzyl bromide | HCID 68527 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Bromo-N,N-dimethylbenzylamine | HCID 235757 | 58% |
Reaction Steps
A solution of 1-bromo-4-(bromomethyl)benzene (20 g, 80.65 mmol, 1.00 equiv), dimethylamine (13.20 g, 96.80 mmol, 1.20 equiv, 33%) and potassium carbonate (13.36 g, 96.81 mmol, 1.20 equiv) in ethanol (200 mL) was stirred overnight at 50° C. The solid material was removed by filtration and the filtrate was concentrated under vacuum. The residue was dissolved in 200 mL of water and extracted with 3×200 mL of dichloromethane. The combined organic layer was washed with 3×200 mL of brine, dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was purified on a silica gel column eluted with dichloromethane/methanol (20:1) to give 10 g (58%) of (4-bromophenyl)-N,N-dimethylmethanamine as a yellow oil. LC-MS: (ES, m/z): 255 [M+CH3CN+H]+, 214 [M+H]+, 169.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09296732B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-6525c9ab545a49f2a385c1c71864515b |
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| Source note | uspto-grants-2016_03 |
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