Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Cumylphenol | HCID 11742 | — |
| Reactant | 3-Pyridinecarbonyl chloride, hydrochloride (1:1) | HCID 88438 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | p-Cumylphenyl nicotinate | HCID 20154093 | — |
Reaction Steps
42,4 g (200 mmol) of p-cumylphenol and 40 g (220 mmol) nicotinic acid chloride hydrochloride was mixed with 600 ml dry pyridine and stirred for 24 hours at 40° C. After cooling precipitated pyridine hydrochloride was sucked off and the filtrate mixed with 150 ml of water. The precipitated raw product was washed with two 100 ml portions of water and recrystallized from methanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04412998 |
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| Source dataset | uspto-grants-1983_11 |
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| ORD ID | ord-832162a2fb0c4992b70214cfe7fb235c |
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| Source note | uspto-grants-1983_11 |
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