HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 611097Generated: October 30, 2026
Dimethylamine → 1-(2-dimethylaminomethyl-6,7-dihydro-4H-furo[3,2-c]pyridin-5-yl)-4-phenylbutan-1-one
https://huagongshe.com/reaction/611097
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | 1-(6,7-dihydro-4H-furo[3,2-c]pyridin-5-yl)-4-phenylbutan-1-one | HCID 19600017 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 1-(2-dimethylaminomethyl-6,7-dihydro-4H-furo[3,2-c]pyridin-5-yl)-4-phenylbutan-1-one | HCID 19599882 | — |
Reaction Steps
To a solution of 0.160 g (0.594 mmol) of 1-(6,7-dihydro-4H-furo[3,2-c]pyridin-5-yl)-4-phenylbutan-1-one in 20 ml of acetic acid, 0.080 ml (0.88 mmol) of 50% aqueous dimethylamine and 0.072 ml (0.88 mmol) of 37% aqueous formaldehyde were added, followed by stirring at 100° C. for 30 minutes. After the solvent was distilled off under reduced pressure, the residual solution was alkalified with aqueous sodium hydroxide and extracted with dichloromethane 2 times. The combined organic layer was washed with water and dried over anhydrous sodium sulfate; the solvent was distilled off under reduced pressure. The resulting crude product was purified by silica gel column chromatography (ethyl acetate to ethyl acetate/methanol=4/1) to yield the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05998433 |
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| Source dataset | uspto-grants-1999_12 |
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| ORD ID | ord-b8a66e8e970343379a9da532f08f65bb |
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| Source note | uspto-grants-1999_12 |
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