HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 544517Generated: October 26, 2026
N-Methylbenzylamine → 2-(N-benzyl-N-methylamino)-1-(2-furyl)ethanol
https://huagongshe.com/reaction/544517
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Methylbenzylamine | HCID 7669 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Bromo-1-(furan-2-yl)ethan-1-one | HCID 2795076 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-(N-benzyl-N-methylamino)-1-(2-furyl)ethanol | HCID 13317251 | 68.8% |
Reaction Steps
2-(Bromoacetyl)furan (95 g) is added slowly to a stirred mixture of 75 g of N-methylbenzylamine and 70 g of potassium carbonate in 300 ml of methanol at 20°-30° C. The mixture is stirred at room temperature for 2.5 hours, and the insoluble matter is filtered off. To the filtrate is added 20 g of sodium borohydride at 10°-20° C. with stirring, and the mixture is stirred at room temperature for 3 hours. The solvent is then distilled off under reduced pressure, water is added to the residue, and the separated oil is extracted with ethyl acetate. The extract is washed with water, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. Distillation of the residue gives 80 g of 2-(N-benzyl-N-methylamino)-1-(2-furyl)ethanol as pale yellow viscous oil, boiling at 130°-138° C. (0.2 mmHg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04450165 |
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| Source dataset | uspto-grants-1984_05 |
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| ORD ID | ord-6f9134d21a2f493cae0b3a9f72c341c1 |
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| Source note | uspto-grants-1984_05 |
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