HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 354717Generated: October 30, 2026
Formaldehyde → 1,3-Dioxan-5-yl 3-pyridyl ketone
https://huagongshe.com/reaction/354717
Participants
| Role | Name | HCID | Charge |
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| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | 3-Acetylpyridine | HCID 9589 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 1,3-Dioxan-5-yl 3-pyridyl ketone | HCID 11970996 | — |
Reaction Steps
A 60.6 g. portion of 3-acetylpyridine was combined with 54 g. of paraformaldehyde and 250 ml. of acetic acid. The mixture was cooled in an ice bath, and 184 ml. (1.5 moles) of boron trifluoride etherate was added dropwise with stirring, over a period of about 40 minutes. The temperature of the mixture ranged from 15° to 26° during the addition. The mixture was then stirred under reflux, at about 67°, for 2 hours 15 minutes, and was then cooled slightly. The volatile portions and most of the acetic acid were removed under vacuum, and the remaining mixture was rinsed with water to a large beaker and was made basic with ammonium hydroxide. The basic mixture was filtered through glass wool, and the filtrate was extracted with chloroform. The organic layer was then washed with saturated aqueous sodium chloride, and was dried over magnesium sulfate and filtered. The filtrate was evaporated under vacuum to obtain 128 g. of crude product, which was recrystallized from isopropanol. The total yield was 59.1 g. of purified product, the first crop of which had a melting point of 98°-100°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04376860 |
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| Source dataset | uspto-grants-1983_03 |
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| ORD ID | ord-bd7291a53dde4e17b1cf1d7c5dddc4ca |
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| Source note | uspto-grants-1983_03 |
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