HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1478657Generated: October 31, 2026
Dimethylformamide → HCID 131728949, compound
https://huagongshe.com/reaction/1478657
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 3-Methoxyphenethylamine | HCID 74866 | — |
| Reactant | Bromomethylstyrene | HCID 98116 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 131728949 | HCID 131728949 | 58% |
Reaction Steps
To a mixture of (3-methoxybenzyl)methylamine (3.02 g, 20 mmol) and cesium carbonate (7.82 g, 24 mmol) in DMF (50 mL) was added cinnamyl bromide (4.47 g, 22 mmol). The reaction mixture was stirred at room temperature for 15 hours. The reaction mixture was diluted with water and extracted with 1:1 hexanes/ethyl acetate (3×). The combined organic extracts were washed with brine, dried over anhydrous sodium sulfate, and concentrated to provide the desired product (3.1 g, 58%): 1H NMR (CDCl3, 500 MHz) δ 7.39-7.37 (m, 2H), 7.32-7.29 (m, 2H), 7.23-7.20 (m, 2H), 6.93-6.91 (m, 2H), 6.81-6.78 (m, 1H), 6.54 (d, J=15.9 Hz, 1H), 6.31 (dt, J=15.9, 6.6 Hz, 1H), 3.81 (s, 3H), 3.52 (s, 2H), 3.19 (dd, J=6.6, 1.2 Hz, 2H), 2.25 (s, 3H); ESI MS m/z=268 [M+H]+. This crude product was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09403776B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-4d053091c5d140f190bd2994ce808d3e |
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| Source note | uspto-grants-2016_08 |
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