Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 1-Dodecanethiol | HCID 8195 | — |
| Reactant | Crotonaldehyde | HCID 447466 | — |
| Product | HCID 86734065 | HCID 86734065 | 90% |
Reaction Steps
0.02 gm Piperidine (catalyst) was dissolved in 30 ml diethyl ether, 0.5 mole lauryl mercaptan was added and the mixture was cooled to 10° C. To this mixture was added 0.5 mole of crotonaldehyde, the rate of addition being such that the reaction temperature never exceeded 10° C. After the addition was completed, the reaction mixture was maintained at a temperature of less than 10° C for a further 60 hours. The reaction mixture was kept under a blanket of nitrogen throughout the preparation. The product β-lauryl-mercaptobutyraldehyde was then obtained by distillation of the mixture under reduced pressure, the product being the fraction of boiling point 154°-155° C at 3 mm Hg pressure. The yield was 90%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03985710 |
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| Source dataset | uspto-grants-1976_10 |
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| ORD ID | ord-ebc7ee88cfea47c09361971abc68e60d |
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| Source note | uspto-grants-1976_10 |
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