Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | (Phenylsulfonyl)acetic acid | HCID 59543 | — |
| Reactant | Piperidin-4-ol | HCID 79341 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 20296624 | HCID 20296624 | — |
Reaction Steps
4.0 g. (0.02 mole) of phenylsulfonylacetic acid was dissolved in 15 ml. of dioxane followed by a solution of 2.0 g. (0.02 mole) of 4-hydroxypiperidine in 20 ml. of dioxane and 2 ml. of water. At 30° C. 3.5 g. (0.04 mole) of 37% aqueous formaldehyde was added rapidly and the reaction mixture agitated thoroughly. The temperature was gradually raised by means of an oil bath to 42° C. and carbon dioxide evolution was initiated. The mixture was maintained at approximately 42° C. for an additional 2 hours. The solvent was removed under reduced pressure and the product was obtained as a residue.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04244963 |
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| Source dataset | uspto-grants-1981_01 |
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| ORD ID | ord-c27cbc0488434fc68ca6a7475223f3a2 |
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| Source note | uspto-grants-1981_01 |
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