HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1356823Generated: October 25, 2026
Methylamine → N-methyl-3-phenylprop-2-en-1-amine
https://huagongshe.com/reaction/1356823
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzene, (3-chloro-1-propenyl)- | HCID 94242 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-methyl-3-phenylprop-2-en-1-amine | HCID 189183 | 83% |
Reaction Steps
Triethylamine (0.66 g; 6.55 mmol) was added to 40% solution of methylamine in methanol (20 ml). While the mixture was stirred at room temperature, cinnamyl chloride (1.00 g; 6.55 mmol) was added dropwise. After completion of the addition, the mixture was stirred for 20 hours at room temperature, and excess methylamine and methanol were removed under reduced pressure. The residue was taken up in a mixture of diethyl ether and 2N hydrochloric acid (100 ml-100 ml), and the aqueous layer was neutralized with aqueous sodium hydroxide solution, followed by extraction with chloroform (100 ml). The organic layer was washed with saturated aqueous sodium bicarbonate solution and then with saturated brine, and dried over sodium sulfate. The solvent was evaporated under reduced pressure, to thereby yield 0.80 g of the target compound as yellow oily matter (yield: 83.0%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06586633B1 |
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| Source dataset | uspto-grants-2003_07 |
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| ORD ID | ord-6ccf9d5ec7cd452e89cc8c4b5df5ac97 |
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| Source note | uspto-grants-2003_07 |
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