HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1606677Generated: November 1, 2026
Pyridine → 19-Chloro-6-methylnonadeca-6,9,12-triene
https://huagongshe.com/reaction/1606677
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 1-Chloro-14-methyl-nonadeca-7,10-diyn-13-ene | HCID 53649475 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Water | HCID 962 | — |
| Product | 19-Chloro-6-methylnonadeca-6,9,12-triene | HCID 54439458 | — |
Reaction Steps
A mixture of 11.0 g. of 1-chloro-14-methyl-nonadeca-7,10-diyn-13-ene, 1.5 g. of 5% palladium on barium sulfate, and 80 ml. of pyridine was shaken in a Parr rocker under 40 lb. of hydrogen pressure for about 1.3 hrs., at which time two moles of hydrogen had been absorbed. The reaction mixture was then poured into water and extracted with ether. The extract was washed with water, dilute hydrochloric acid, saturated aqueous sodium chloride, dried over sodium sulfate, and evaporated leaving a residue comprising 1-chloro-14-methyl-7,10,13-nonadecatriene. The residue was distilled in a rocking short-path distillation apparatus, collecting 7.6 g. of a mixture comprising 1-chloro-14-methyl-7,10,13-nonadecatriene at a bath temperature of 180°C. and a pressure of 0.005 mm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03953499 |
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| Source dataset | uspto-grants-1976_04 |
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| ORD ID | ord-604faddc693448ffa6a8516f21b8fb9c |
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| Source note | uspto-grants-1976_04 |
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