Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | HCID 19600258 | HCID 19600258 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 19600154 | HCID 19600154 | — |
Reaction Steps
To a solution of 1.803 g (10.912 mmol) of N-allyl-3-(3-furyl)propylamine in 50 ml of acetic acid, 1.06 g (13.1 mmol) of 37% aqueous formaldehyde was added, followed by stirring at 100° C. for 1 hour. After the solvent was distilled off under reduced pressure, the residual solution was alkalified with aqueous sodium hydroxide, and extracted with dichloromethane 3 times. The combined organic layer was dried over anhydrous magnesium sulfate; the solvent was distilled off under reduced pressure. The resulting crude product was purified by silica gel column chromatography (hexane/ethyl acetate=6/1 to 3/1) 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-6ba0edb31d5a4bf78a3c385548071f03 |
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| Source note | uspto-grants-1999_12 |
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