Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 4-Methylbenzaldehyde | HCID 7725 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Phenylsulphonylacetonitrile | HCID 82077 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 5067622 | HCID 5067622 | — |
Reaction Steps
120 g (1 mole) of p-methylbenzaldehyde were heated to the boil on a water separator and under reflux with 181 g (1 mole) of phenylsulfonyl-acetonitrile in 500 ml benzene with addition of 6 ml of piperidine and 3 ml of glacial acetic acid. After 5 hours, 17 ml water had separated. Upon cooling to 10° C, the 1-p-tolyl-2-cyano-2-phenylsulfonyl-ethlene crystallized; after suction filtration, washing with 150 ml of cold benzene and drying, 206 g (73% of the theory) were obtained; melting point: 145°-147° C. ##STR14##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04001221 |
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| Source dataset | uspto-grants-1977_01 |
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| ORD ID | ord-c74855fa121342b7bcbd38b2cb8c4f3d |
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| Source note | uspto-grants-1977_01 |
|---|