HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → HCID 69535235, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Phenylsulphonylacetonitrile | HCID 82077 | — |
| Reactant | 4-[(2-Methylprop-2-en-1-yl)oxy]benzaldehyde | HCID 13203751 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 69535235 | HCID 69535235 | 77% |
Reaction Steps
A solution of 4-(2-methylallyloxy)-benzaldehyde (7.03 g, 40 mmol) and of (phenylsulfonyl)acetonitrile (7.24 g, 40 mmol) in 70 ml absolute ethanol is heated under reflux in the presence of a catalytic quantity of piperidine (0.5 ml) for 48 hours. The reaction medium is cooled to room temperature and the precipitate formed is filtered and washed with cold ethanol. After drying in a dessicator, 10.45 g (yield 77%) of 2-benzenesulfonyl-3-[4-(2-methylallyloxy)phenyl]acrylonitrile are obtained in the form of a very pale yellow solid which is used as it is in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07138108B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-6b89454ad4cb48a09e5a8b203db011a3 |
| Source note | uspto-grants-2006_11 |